Canonical Allele Identifier: CA1941472795

Gene: HTRA1

Linked Data

• dbSNP Id: rs2097498977

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122496959G>C , CM000672.2:g.122496959G>C	GRCh38
NC_000010.10:g.124256475G>C , CM000672.1:g.124256475G>C	GRCh37
NC_000010.9:g.124246465G>C	NCBI36
NG_011554.1:g.40435G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.777+7333G>C MANE Select	ENSP00000357980.3:n.777+7333G>C
ENST00000648167.1:c.459+7333G>C	ENSP00000498033.1:n.459+7333G>C
ENST00000368984.7:c.777+7333G>C	ENSP00000357980.3:n.777+7333G>C
NM_002775.4:c.777+7333G>C	NP_002766.1:n.777+7333G>C
NM_002775.5:c.777+7333G>C MANE Select	NP_002766.1:n.777+7333G>C