Canonical Allele Identifier: CA660871611

Gene: HTRA1

Linked Data

• dbSNP Id: rs1457859430
• MyVariant Identifiers: chr10:g.124231548G>T (hg19) ; chr10:g.122472032G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122472032G>T , CM000672.2:g.122472032G>T	GRCh38
NC_000010.10:g.124231548G>T , CM000672.1:g.124231548G>T	GRCh37
NC_000010.9:g.124221538G>T	NCBI36
NG_011554.1:g.15508G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.472+9908G>T MANE Select	ENSP00000357980.3:n.472+9908G>T
ENST00000648167.1:c.154+13323G>T	ENSP00000498033.1:n.154+13323G>T
ENST00000368984.7:c.472+9908G>T	ENSP00000357980.3:n.472+9908G>T
NM_002775.4:c.472+9908G>T	NP_002766.1:n.472+9908G>T
NM_002775.5:c.472+9908G>T MANE Select	NP_002766.1:n.472+9908G>T