Canonical Allele Identifier: CA378585444
Gene: HTRA1 HGNC NCBI

Linked Data

gnomAD v4: 10-122506747-C-A
MyVariant Identifiers: chr10:g.124266263C>A (hg19) chr10:g.122506747C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506747C>A , CM000672.2:g.122506747C>A GRCh38
NC_000010.10:g.124266263C>A , CM000672.1:g.124266263C>A GRCh37
NC_000010.9:g.124256253C>A NCBI36
NG_011554.1:g.50223C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.834C>A MANE Select ENSP00000357980.3:p.Phe278Leu
ENST00000648167.1:c.516C>A ENSP00000498033.1:p.Phe172Leu
ENST00000368984.7:c.834C>A ENSP00000357980.3:p.Phe278Leu
ENST00000420892.1:c.57C>A ENSP00000412676.1:p.Phe19Leu
NM_002775.4:c.834C>A NP_002766.1:p.Phe278Leu
NM_002775.5:c.834C>A MANE Select NP_002766.1:p.Phe278Leu
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