Canonical Allele Identifier: CA343773692
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878791T>C (hg19) chr1:g.173909653T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909653T>C , CM000663.2:g.173909653T>C GRCh38
NC_000001.10:g.173878791T>C , CM000663.1:g.173878791T>C GRCh37
NC_000001.9:g.172145414T>C NCBI36
NG_012462.1:g.12726A>G , LRG_577:g.12726A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1052A>G MANE Select ENSP00000356671.3:p.His351Arg
ENST00000367698.3:c.1052A>G ENSP00000356671.3:p.His351Arg
ENST00000617423.4:c.560-2160A>G ENSP00000478688.1:n.560-2160A>G
NM_000488.3:c.1052A>G , LRG_577t1:c.1052A>G NP_000479.1:p.His351Arg
XM_005245198.2:c.908A>G XP_005245255.1:p.His303Arg
NM_001365052.1:c.908A>G NP_001351981.1:p.His303Arg
NM_000488.4:c.1052A>G MANE Select NP_000479.1:p.His351Arg
NM_001365052.2:c.908A>G NP_001351981.1:p.His303Arg
NM_001386302.1:c.1175A>G NP_001373231.1:p.His392Arg
NM_001386303.1:c.1133A>G NP_001373232.1:p.His378Arg
NM_001386304.1:c.1031A>G NP_001373233.1:p.His344Arg
NM_001386305.1:c.995A>G NP_001373234.1:p.His332Arg
NM_001386306.1:c.836A>G NP_001373235.1:p.His279Arg
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