Canonical Allele Identifier: CA471745311
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124221198G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461682G>T , CM000672.2:g.122461682G>T GRCh38
NC_000010.10:g.124221198G>T , CM000672.1:g.124221198G>T GRCh37
NC_000010.9:g.124211188G>T NCBI36
NG_011554.1:g.5158G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.30G>T MANE Select ENSP00000357980.3:p.Pro10=
ENST00000648167.1:c.154+2973G>T ENSP00000498033.1:n.154+2973G>T
ENST00000368984.7:c.30G>T ENSP00000357980.3:p.Pro10=
NM_002775.4:c.30G>T NP_002766.1:p.Pro10=
NM_002775.5:c.30G>T MANE Select NP_002766.1:p.Pro10=