Canonical Allele Identifier: CA660910258
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1184857444
gnomAD v4: 10-122506579-G-A
MyVariant Identifiers: chr10:g.124266095G>A (hg19) chr10:g.122506579G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506579G>A , CM000672.2:g.122506579G>A GRCh38
NC_000010.10:g.124266095G>A , CM000672.1:g.124266095G>A GRCh37
NC_000010.9:g.124256085G>A NCBI36
NG_011554.1:g.50055G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.778-112G>A MANE Select ENSP00000357980.3:n.778-112G>A
ENST00000648167.1:c.460-112G>A ENSP00000498033.1:n.460-112G>A
ENST00000368984.7:c.778-112G>A ENSP00000357980.3:n.778-112G>A
NM_002775.4:c.778-112G>A NP_002766.1:n.778-112G>A
NM_002775.5:c.778-112G>A MANE Select NP_002766.1:n.778-112G>A
Search 100 bp 5'
Search 100 bp 3'