Canonical Allele Identifier: CA471666779
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124266278A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506762A>C , CM000672.2:g.122506762A>C GRCh38
NC_000010.10:g.124266278A>C , CM000672.1:g.124266278A>C GRCh37
NC_000010.9:g.124256268A>C NCBI36
NG_011554.1:g.50238A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.849A>C MANE Select ENSP00000357980.3:p.Gly283=
ENST00000648167.1:c.531A>C ENSP00000498033.1:p.Gly177=
ENST00000368984.7:c.849A>C ENSP00000357980.3:p.Gly283=
ENST00000420892.1:c.72A>C ENSP00000412676.1:p.Gly24=
NM_002775.4:c.849A>C NP_002766.1:p.Gly283=
NM_002775.5:c.849A>C MANE Select NP_002766.1:p.Gly283=
Search 100 bp 5'
Search 100 bp 3'