Canonical Allele Identifier: CA660865482

Gene: HTRA1

Linked Data

• dbSNP Id: rs1212745468
• gnomAD v4: 10-122461519-C-T
• MyVariant Identifiers: chr10:g.124221035C>T (hg19) ; chr10:g.122461519C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122461519C>T , CM000672.2:g.122461519C>T	GRCh38
NC_000010.10:g.124221035C>T , CM000672.1:g.124221035C>T	GRCh37
NC_000010.9:g.124211025C>T	NCBI36
NG_011554.1:g.4995C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000648167.1:c.154+2810C>T	ENSP00000498033.1:n.154+2810C>T