Canonical Allele Identifier: CA378585584
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124266297A>G (hg19) chr10:g.122506781A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506781A>G , CM000672.2:g.122506781A>G GRCh38
NC_000010.10:g.124266297A>G , CM000672.1:g.124266297A>G GRCh37
NC_000010.9:g.124256287A>G NCBI36
NG_011554.1:g.50257A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.868A>G MANE Select ENSP00000357980.3:p.Asn290Asp
ENST00000648167.1:c.550A>G ENSP00000498033.1:p.Asn184Asp
ENST00000368984.7:c.868A>G ENSP00000357980.3:p.Asn290Asp
ENST00000420892.1:c.91A>G ENSP00000412676.1:p.Asn31Asp
NM_002775.4:c.868A>G NP_002766.1:p.Asn290Asp
NM_002775.5:c.868A>G MANE Select NP_002766.1:p.Asn290Asp
Search 100 bp 5'
Search 100 bp 3'