Canonical Allele Identifier: CA471745300
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124221192T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461676T>C , CM000672.2:g.122461676T>C GRCh38
NC_000010.10:g.124221192T>C , CM000672.1:g.124221192T>C GRCh37
NC_000010.9:g.124211182T>C NCBI36
NG_011554.1:g.5152T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.24T>C MANE Select ENSP00000357980.3:p.Leu8=
ENST00000648167.1:c.154+2967T>C ENSP00000498033.1:n.154+2967T>C
ENST00000368984.7:c.24T>C ENSP00000357980.3:p.Leu8=
NM_002775.4:c.24T>C NP_002766.1:p.Leu8=
NM_002775.5:c.24T>C MANE Select NP_002766.1:p.Leu8=