Canonical Allele Identifier: CA343774663
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879022G>C (hg19) chr1:g.173909884G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909884G>C , CM000663.2:g.173909884G>C GRCh38
NC_000001.10:g.173879022G>C , CM000663.1:g.173879022G>C GRCh37
NC_000001.9:g.172145645G>C NCBI36
NG_012462.1:g.12495C>G , LRG_577:g.12495C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.821C>G MANE Select ENSP00000356671.3:p.Ala274Gly
ENST00000367698.3:c.821C>G ENSP00000356671.3:p.Ala274Gly
ENST00000487183.1:n.472C>G
ENST00000617423.4:c.559+1980C>G ENSP00000478688.1:n.559+1980C>G
NM_000488.3:c.821C>G , LRG_577t1:c.821C>G NP_000479.1:p.Ala274Gly
XM_005245198.2:c.677C>G XP_005245255.1:p.Ala226Gly
NM_001365052.1:c.677C>G NP_001351981.1:p.Ala226Gly
NM_000488.4:c.821C>G MANE Select NP_000479.1:p.Ala274Gly
NM_001365052.2:c.677C>G NP_001351981.1:p.Ala226Gly
NM_001386302.1:c.944C>G NP_001373231.1:p.Ala315Gly
NM_001386303.1:c.902C>G NP_001373232.1:p.Ala301Gly
NM_001386304.1:c.800C>G NP_001373233.1:p.Ala267Gly
NM_001386305.1:c.764C>G NP_001373234.1:p.Ala255Gly
NM_001386306.1:c.605C>G NP_001373235.1:p.Ala202Gly
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