Canonical Allele Identifier: CA421821591
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873168G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904030G>C , CM000663.2:g.173904030G>C GRCh38
NC_000001.10:g.173873168G>C , CM000663.1:g.173873168G>C GRCh37
NC_000001.9:g.172139791G>C NCBI36
NG_012462.1:g.18349C>G , LRG_577:g.18349C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1254C>G MANE Select ENSP00000356671.3:p.Thr418=
ENST00000367698.3:c.1254C>G ENSP00000356671.3:p.Thr418=
ENST00000617423.4:c.639C>G ENSP00000478688.1:p.Thr213=
NM_000488.3:c.1254C>G , LRG_577t1:c.1254C>G NP_000479.1:p.Thr418=
XM_005245198.2:c.1110C>G XP_005245255.1:p.Thr370=
NM_001365052.1:c.1110C>G NP_001351981.1:p.Thr370=
NM_000488.4:c.1254C>G MANE Select NP_000479.1:p.Thr418=
NM_001365052.2:c.1110C>G NP_001351981.1:p.Thr370=
NM_001386302.1:c.1377C>G NP_001373231.1:p.Thr459=
NM_001386303.1:c.1335C>G NP_001373232.1:p.Thr445=
NM_001386304.1:c.1233C>G NP_001373233.1:p.Thr411=
NM_001386305.1:c.1197C>G NP_001373234.1:p.Thr399=
NM_001386306.1:c.1038C>G NP_001373235.1:p.Thr346=
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