Canonical Allele Identifier: CA1941472705
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs2097498911

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122496741A>G , CM000672.2:g.122496741A>G GRCh38
NC_000010.10:g.124256257A>G , CM000672.1:g.124256257A>G GRCh37
NC_000010.9:g.124246247A>G NCBI36
NG_011554.1:g.40217A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.777+7115A>G MANE Select ENSP00000357980.3:n.777+7115A>G
ENST00000648167.1:c.459+7115A>G ENSP00000498033.1:n.459+7115A>G
ENST00000368984.7:c.777+7115A>G ENSP00000357980.3:n.777+7115A>G
NM_002775.4:c.777+7115A>G NP_002766.1:n.777+7115A>G
NM_002775.5:c.777+7115A>G MANE Select NP_002766.1:n.777+7115A>G