Canonical Allele Identifier: CA660871879

Gene: HTRA1

Linked Data

• dbSNP Id: rs1238085006
• MyVariant Identifiers: chr10:g.124231887A>T (hg19) ; chr10:g.122472371A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122472371A>T , CM000672.2:g.122472371A>T	GRCh38
NC_000010.10:g.124231887A>T , CM000672.1:g.124231887A>T	GRCh37
NC_000010.9:g.124221877A>T	NCBI36
NG_011554.1:g.15847A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.472+10247A>T MANE Select	ENSP00000357980.3:n.472+10247A>T
ENST00000648167.1:c.154+13662A>T	ENSP00000498033.1:n.154+13662A>T
ENST00000368984.7:c.472+10247A>T	ENSP00000357980.3:n.472+10247A>T
NM_002775.4:c.472+10247A>T	NP_002766.1:n.472+10247A>T
NM_002775.5:c.472+10247A>T MANE Select	NP_002766.1:n.472+10247A>T