Canonical Allele Identifier: CA343774264
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878926A>C (hg19) chr1:g.173909788A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909788A>C , CM000663.2:g.173909788A>C GRCh38
NC_000001.10:g.173878926A>C , CM000663.1:g.173878926A>C GRCh37
NC_000001.9:g.172145549A>C NCBI36
NG_012462.1:g.12591T>G , LRG_577:g.12591T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.917T>G MANE Select ENSP00000356671.3:p.Phe306Cys
ENST00000367698.3:c.917T>G ENSP00000356671.3:p.Phe306Cys
ENST00000487183.1:n.568T>G
ENST00000617423.4:c.559+2076T>G ENSP00000478688.1:n.559+2076T>G
NM_000488.3:c.917T>G , LRG_577t1:c.917T>G NP_000479.1:p.Phe306Cys
XM_005245198.2:c.773T>G XP_005245255.1:p.Phe258Cys
NM_001365052.1:c.773T>G NP_001351981.1:p.Phe258Cys
NM_000488.4:c.917T>G MANE Select NP_000479.1:p.Phe306Cys
NM_001365052.2:c.773T>G NP_001351981.1:p.Phe258Cys
NM_001386302.1:c.1040T>G NP_001373231.1:p.Phe347Cys
NM_001386303.1:c.998T>G NP_001373232.1:p.Phe333Cys
NM_001386304.1:c.896T>G NP_001373233.1:p.Phe299Cys
NM_001386305.1:c.860T>G NP_001373234.1:p.Phe287Cys
NM_001386306.1:c.701T>G NP_001373235.1:p.Phe234Cys
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