Canonical Allele Identifier: CA378586903
Gene: HTRA1 HGNC NCBI

Linked Data

gnomAD v4: 10-122508755-G-A
MyVariant Identifiers: chr10:g.124268271G>A (hg19) chr10:g.122508755G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508755G>A , CM000672.2:g.122508755G>A GRCh38
NC_000010.10:g.124268271G>A , CM000672.1:g.124268271G>A GRCh37
NC_000010.9:g.124258261G>A NCBI36
NG_011554.1:g.52231G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1105G>A MANE Select ENSP00000357980.3:p.Asp369Asn
ENST00000648167.1:c.787G>A ENSP00000498033.1:p.Asp263Asn
ENST00000368984.7:c.1105G>A ENSP00000357980.3:p.Asp369Asn
ENST00000420892.1:c.328G>A ENSP00000412676.1:p.Asp110Asn
NM_002775.4:c.1105G>A NP_002766.1:p.Asp369Asn
NM_002775.5:c.1105G>A MANE Select NP_002766.1:p.Asp369Asn
Search 100 bp 5'
Search 100 bp 3'