Canonical Allele Identifier: CA378605889
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1202206275
gnomAD v2: 10-124221388-G-A
gnomAD v4: 10-122461872-G-A
MyVariant Identifiers: chr10:g.124221388G>A (hg19) chr10:g.122461872G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461872G>A , CM000672.2:g.122461872G>A GRCh38
NC_000010.10:g.124221388G>A , CM000672.1:g.124221388G>A GRCh37
NC_000010.9:g.124211378G>A NCBI36
NG_011554.1:g.5348G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.220G>A MANE Select ENSP00000357980.3:p.Ala74Thr
ENST00000648167.1:c.154+3163G>A ENSP00000498033.1:n.154+3163G>A
ENST00000368984.7:c.220G>A ENSP00000357980.3:p.Ala74Thr
NM_002775.4:c.220G>A NP_002766.1:p.Ala74Thr
NM_002775.5:c.220G>A MANE Select NP_002766.1:p.Ala74Thr
Search 100 bp 5'
Search 100 bp 3'