Canonical Allele Identifier: CA343774293
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878933A>C (hg19) chr1:g.173909795A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909795A>C , CM000663.2:g.173909795A>C GRCh38
NC_000001.10:g.173878933A>C , CM000663.1:g.173878933A>C GRCh37
NC_000001.9:g.172145556A>C NCBI36
NG_012462.1:g.12584T>G , LRG_577:g.12584T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.910T>G MANE Select ENSP00000356671.3:p.Leu304Val
ENST00000367698.3:c.910T>G ENSP00000356671.3:p.Leu304Val
ENST00000487183.1:n.561T>G
ENST00000617423.4:c.559+2069T>G ENSP00000478688.1:n.559+2069T>G
NM_000488.3:c.910T>G , LRG_577t1:c.910T>G NP_000479.1:p.Leu304Val
XM_005245198.2:c.766T>G XP_005245255.1:p.Leu256Val
NM_001365052.1:c.766T>G NP_001351981.1:p.Leu256Val
NM_000488.4:c.910T>G MANE Select NP_000479.1:p.Leu304Val
NM_001365052.2:c.766T>G NP_001351981.1:p.Leu256Val
NM_001386302.1:c.1033T>G NP_001373231.1:p.Leu345Val
NM_001386303.1:c.991T>G NP_001373232.1:p.Leu331Val
NM_001386304.1:c.889T>G NP_001373233.1:p.Leu297Val
NM_001386305.1:c.853T>G NP_001373234.1:p.Leu285Val
NM_001386306.1:c.694T>G NP_001373235.1:p.Leu232Val
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