Canonical Allele Identifier: CA378606180
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124221496T>G (hg19) chr10:g.122461980T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461980T>G , CM000672.2:g.122461980T>G GRCh38
NC_000010.10:g.124221496T>G , CM000672.1:g.124221496T>G GRCh37
NC_000010.9:g.124211486T>G NCBI36
NG_011554.1:g.5456T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.328T>G MANE Select ENSP00000357980.3:p.Cys110Gly
ENST00000648167.1:c.154+3271T>G ENSP00000498033.1:n.154+3271T>G
ENST00000368984.7:c.328T>G ENSP00000357980.3:p.Cys110Gly
NM_002775.4:c.328T>G NP_002766.1:p.Cys110Gly
NM_002775.5:c.328T>G MANE Select NP_002766.1:p.Cys110Gly
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