Canonical Allele Identifier: CA343774692
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879028T>C (hg19) chr1:g.173909890T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909890T>C , CM000663.2:g.173909890T>C GRCh38
NC_000001.10:g.173879028T>C , CM000663.1:g.173879028T>C GRCh37
NC_000001.9:g.172145651T>C NCBI36
NG_012462.1:g.12489A>G , LRG_577:g.12489A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.815A>G MANE Select ENSP00000356671.3:p.Tyr272Cys
ENST00000367698.3:c.815A>G ENSP00000356671.3:p.Tyr272Cys
ENST00000487183.1:n.466A>G
ENST00000617423.4:c.559+1974A>G ENSP00000478688.1:n.559+1974A>G
NM_000488.3:c.815A>G , LRG_577t1:c.815A>G NP_000479.1:p.Tyr272Cys
XM_005245198.2:c.671A>G XP_005245255.1:p.Tyr224Cys
NM_001365052.1:c.671A>G NP_001351981.1:p.Tyr224Cys
NM_000488.4:c.815A>G MANE Select NP_000479.1:p.Tyr272Cys
NM_001365052.2:c.671A>G NP_001351981.1:p.Tyr224Cys
NM_001386302.1:c.938A>G NP_001373231.1:p.Tyr313Cys
NM_001386303.1:c.896A>G NP_001373232.1:p.Tyr299Cys
NM_001386304.1:c.794A>G NP_001373233.1:p.Tyr265Cys
NM_001386305.1:c.763-5A>G NP_001373234.1:n.763-5A>G
NM_001386306.1:c.599A>G NP_001373235.1:p.Tyr200Cys
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