Canonical Allele Identifier: CA343773697
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878792G>C (hg19) chr1:g.173909654G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909654G>C , CM000663.2:g.173909654G>C GRCh38
NC_000001.10:g.173878792G>C , CM000663.1:g.173878792G>C GRCh37
NC_000001.9:g.172145415G>C NCBI36
NG_012462.1:g.12725C>G , LRG_577:g.12725C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1051C>G MANE Select ENSP00000356671.3:p.His351Asp
ENST00000367698.3:c.1051C>G ENSP00000356671.3:p.His351Asp
ENST00000617423.4:c.560-2161C>G ENSP00000478688.1:n.560-2161C>G
NM_000488.3:c.1051C>G , LRG_577t1:c.1051C>G NP_000479.1:p.His351Asp
XM_005245198.2:c.907C>G XP_005245255.1:p.His303Asp
NM_001365052.1:c.907C>G NP_001351981.1:p.His303Asp
NM_000488.4:c.1051C>G MANE Select NP_000479.1:p.His351Asp
NM_001365052.2:c.907C>G NP_001351981.1:p.His303Asp
NM_001386302.1:c.1174C>G NP_001373231.1:p.His392Asp
NM_001386303.1:c.1132C>G NP_001373232.1:p.His378Asp
NM_001386304.1:c.1030C>G NP_001373233.1:p.His344Asp
NM_001386305.1:c.994C>G NP_001373234.1:p.His332Asp
NM_001386306.1:c.835C>G NP_001373235.1:p.His279Asp
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