Canonical Allele Identifier: CA471745290

Gene: HTRA1

Linked Data

• gnomAD v4: 10-122461670-C-G
• MyVariant Identifiers: chr10:g.124221186C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122461670C>G , CM000672.2:g.122461670C>G	GRCh38
NC_000010.10:g.124221186C>G , CM000672.1:g.124221186C>G	GRCh37
NC_000010.9:g.124211176C>G	NCBI36
NG_011554.1:g.5146C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368984.8:c.18C>G MANE Select	ENSP00000357980.3:p.Ala6=
ENST00000648167.1:c.154+2961C>G	ENSP00000498033.1:n.154+2961C>G
ENST00000368984.7:c.18C>G	ENSP00000357980.3:p.Ala6=
NM_002775.4:c.18C>G	NP_002766.1:p.Ala6=
NM_002775.5:c.18C>G MANE Select	NP_002766.1:p.Ala6=