Canonical Allele Identifier: CA343772144
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1657367308
MyVariant Identifiers: chr1:g.173873063G>C (hg19) chr1:g.173903925G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903925G>C , CM000663.2:g.173903925G>C GRCh38
NC_000001.10:g.173873063G>C , CM000663.1:g.173873063G>C GRCh37
NC_000001.9:g.172139686G>C NCBI36
NG_012462.1:g.18454C>G , LRG_577:g.18454C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1359C>G MANE Select ENSP00000356671.3:p.Ile453Met
ENST00000367698.3:c.1359C>G ENSP00000356671.3:p.Ile453Met
ENST00000617423.4:c.744C>G ENSP00000478688.1:p.Ile248Met
NM_000488.3:c.1359C>G , LRG_577t1:c.1359C>G NP_000479.1:p.Ile453Met
XM_005245198.2:c.1215C>G XP_005245255.1:p.Ile405Met
NM_001365052.1:c.1215C>G NP_001351981.1:p.Ile405Met
NM_000488.4:c.1359C>G MANE Select NP_000479.1:p.Ile453Met
NM_001365052.2:c.1215C>G NP_001351981.1:p.Ile405Met
NM_001386302.1:c.1482C>G NP_001373231.1:p.Ile494Met
NM_001386303.1:c.1440C>G NP_001373232.1:p.Ile480Met
NM_001386304.1:c.1338C>G NP_001373233.1:p.Ile446Met
NM_001386305.1:c.1302C>G NP_001373234.1:p.Ile434Met
NM_001386306.1:c.1143C>G NP_001373235.1:p.Ile381Met
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