Canonical Allele Identifier: CA471745299
Gene: HTRA1 HGNC NCBI

Linked Data

gnomAD v4: 10-122461676-T-A
MyVariant Identifiers: chr10:g.124221192T>A (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.24T>A MANE Select ENSP00000357980.3:p.Leu8=
ENST00000648167.1:c.154+2967T>A ENSP00000498033.1:n.154+2967T>A
ENST00000368984.7:c.24T>A ENSP00000357980.3:p.Leu8=
NM_002775.4:c.24T>A NP_002766.1:p.Leu8=
NM_002775.5:c.24T>A MANE Select NP_002766.1:p.Leu8=
Search 100 bp 5'
Search 100 bp 3'