Canonical Allele Identifier: CA596578960
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1336713307
gnomAD v2: 10-124221094-C-A
gnomAD v4: 10-122461578-C-A
MyVariant Identifiers: chr10:g.124221094C>A (hg19) chr10:g.122461578C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461578C>A , CM000672.2:g.122461578C>A GRCh38
NC_000010.10:g.124221094C>A , CM000672.1:g.124221094C>A GRCh37
NC_000010.9:g.124211084C>A NCBI36
NG_011554.1:g.5054C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.-75C>A MANE Select ENSP00000357980.3:n.-75C>A
ENST00000648167.1:c.154+2869C>A ENSP00000498033.1:n.154+2869C>A
ENST00000368984.7:c.-75C>A ENSP00000357980.3:n.-75C>A
NM_002775.4:c.-75C>A NP_002766.1:n.-75C>A
NM_002775.5:c.-75C>A MANE Select NP_002766.1:n.-75C>A
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