Canonical Allele Identifier: CA378585352
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs376830136
gnomAD v4: 10-122506728-A-G
MyVariant Identifiers: chr10:g.124266244A>G (hg19) chr10:g.122506728A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506728A>G , CM000672.2:g.122506728A>G GRCh38
NC_000010.10:g.124266244A>G , CM000672.1:g.124266244A>G GRCh37
NC_000010.9:g.124256234A>G NCBI36
NG_011554.1:g.50204A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.815A>G MANE Select ENSP00000357980.3:p.Glu272Gly
ENST00000648167.1:c.497A>G ENSP00000498033.1:p.Glu166Gly
ENST00000368984.7:c.815A>G ENSP00000357980.3:p.Glu272Gly
ENST00000420892.1:c.38A>G ENSP00000412676.1:p.Glu13Gly
NM_002775.4:c.815A>G NP_002766.1:p.Glu272Gly
NM_002775.5:c.815A>G MANE Select NP_002766.1:p.Glu272Gly
Search 100 bp 5'
Search 100 bp 3'