Canonical Allele Identifier: CA343774675
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1657695666
MyVariant Identifiers: chr1:g.173879025T>C (hg19) chr1:g.173909887T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909887T>C , CM000663.2:g.173909887T>C GRCh38
NC_000001.10:g.173879025T>C , CM000663.1:g.173879025T>C GRCh37
NC_000001.9:g.172145648T>C NCBI36
NG_012462.1:g.12492A>G , LRG_577:g.12492A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.818A>G MANE Select ENSP00000356671.3:p.Lys273Arg
ENST00000367698.3:c.818A>G ENSP00000356671.3:p.Lys273Arg
ENST00000487183.1:n.469A>G
ENST00000617423.4:c.559+1977A>G ENSP00000478688.1:n.559+1977A>G
NM_000488.3:c.818A>G , LRG_577t1:c.818A>G NP_000479.1:p.Lys273Arg
XM_005245198.2:c.674A>G XP_005245255.1:p.Lys225Arg
NM_001365052.1:c.674A>G NP_001351981.1:p.Lys225Arg
NM_000488.4:c.818A>G MANE Select NP_000479.1:p.Lys273Arg
NM_001365052.2:c.674A>G NP_001351981.1:p.Lys225Arg
NM_001386302.1:c.941A>G NP_001373231.1:p.Lys314Arg
NM_001386303.1:c.899A>G NP_001373232.1:p.Lys300Arg
NM_001386304.1:c.797A>G NP_001373233.1:p.Lys266Arg
NM_001386305.1:c.763-2A>G NP_001373234.1:n.763-2A>G
NM_001386306.1:c.602A>G NP_001373235.1:p.Lys201Arg
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