Canonical Allele Identifier: CA378605319
Gene: HTRA1 HGNC NCBI

Linked Data

gnomAD v4: 10-122461713-T-A
MyVariant Identifiers: chr10:g.124221229T>A (hg19) chr10:g.122461713T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461713T>A , CM000672.2:g.122461713T>A GRCh38
NC_000010.10:g.124221229T>A , CM000672.1:g.124221229T>A GRCh37
NC_000010.9:g.124211219T>A NCBI36
NG_011554.1:g.5189T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.61T>A MANE Select ENSP00000357980.3:p.Ser21Thr
ENST00000648167.1:c.154+3004T>A ENSP00000498033.1:n.154+3004T>A
ENST00000368984.7:c.61T>A ENSP00000357980.3:p.Ser21Thr
NM_002775.4:c.61T>A NP_002766.1:p.Ser21Thr
NM_002775.5:c.61T>A MANE Select NP_002766.1:p.Ser21Thr
Search 100 bp 5'
Search 100 bp 3'