Canonical Allele Identifier: CA343772709
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1527905
ClinVar RCV Id: RCV002074473
dbSNP Id: rs2102773374
MyVariant Identifiers: chr1:g.173873205T>C (hg19) chr1:g.173904067T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904067T>C , CM000663.2:g.173904067T>C GRCh38
NC_000001.10:g.173873205T>C , CM000663.1:g.173873205T>C GRCh37
NC_000001.9:g.172139828T>C NCBI36
NG_012462.1:g.18312A>G , LRG_577:g.18312A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1219-2A>G MANE Select ENSP00000356671.3:n.1219-2A>G
ENST00000367698.3:c.1219-2A>G ENSP00000356671.3:n.1219-2A>G
ENST00000617423.4:c.604-2A>G ENSP00000478688.1:n.604-2A>G
NM_000488.3:c.1219-2A>G , LRG_577t1:c.1219-2A>G NP_000479.1:n.1219-2A>G
XM_005245198.2:c.1075-2A>G XP_005245255.1:n.1075-2A>G
NM_001365052.1:c.1075-2A>G NP_001351981.1:n.1075-2A>G
NM_000488.4:c.1219-2A>G MANE Select NP_000479.1:n.1219-2A>G
NM_001365052.2:c.1075-2A>G NP_001351981.1:n.1075-2A>G
NM_001386302.1:c.1342-2A>G NP_001373231.1:n.1342-2A>G
NM_001386303.1:c.1300-2A>G NP_001373232.1:n.1300-2A>G
NM_001386304.1:c.1198-2A>G NP_001373233.1:n.1198-2A>G
NM_001386305.1:c.1162-2A>G NP_001373234.1:n.1162-2A>G
NM_001386306.1:c.1003-2A>G NP_001373235.1:n.1003-2A>G
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