Canonical Allele Identifier: CA471745720
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1171399687
gnomAD v2: 10-124221417-C-T
gnomAD v4: 10-122461901-C-T
MyVariant Identifiers: chr10:g.124221417C>T (hg19) chr10:g.122461901C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461901C>T , CM000672.2:g.122461901C>T GRCh38
NC_000010.10:g.124221417C>T , CM000672.1:g.124221417C>T GRCh37
NC_000010.9:g.124211407C>T NCBI36
NG_011554.1:g.5377C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.249C>T MANE Select ENSP00000357980.3:p.Cys83=
ENST00000648167.1:c.154+3192C>T ENSP00000498033.1:n.154+3192C>T
ENST00000368984.7:c.249C>T ENSP00000357980.3:p.Cys83=
NM_002775.4:c.249C>T NP_002766.1:p.Cys83=
NM_002775.5:c.249C>T MANE Select NP_002766.1:p.Cys83=
Search 100 bp 5'
Search 100 bp 3'