Canonical Allele Identifier: CA596578972
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1391239135
gnomAD v2: 10-124221130-G-A
gnomAD v3: 10-122461614-G-A
gnomAD v4: 10-122461614-G-A
MyVariant Identifiers: chr10:g.124221130G>A (hg19) chr10:g.122461614G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461614G>A , CM000672.2:g.122461614G>A GRCh38
NC_000010.10:g.124221130G>A , CM000672.1:g.124221130G>A GRCh37
NC_000010.9:g.124211120G>A NCBI36
NG_011554.1:g.5090G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.-39G>A MANE Select ENSP00000357980.3:n.-39G>A
ENST00000648167.1:c.154+2905G>A ENSP00000498033.1:n.154+2905G>A
ENST00000368984.7:c.-39G>A ENSP00000357980.3:n.-39G>A
NM_002775.4:c.-39G>A NP_002766.1:n.-39G>A
NM_002775.5:c.-39G>A MANE Select NP_002766.1:n.-39G>A
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