Canonical Allele Identifier: CA378586892
Gene: HTRA1 HGNC NCBI

Linked Data

gnomAD v4: 10-122508752-C-G
MyVariant Identifiers: chr10:g.124268268C>G (hg19) chr10:g.122508752C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508752C>G , CM000672.2:g.122508752C>G GRCh38
NC_000010.10:g.124268268C>G , CM000672.1:g.124268268C>G GRCh37
NC_000010.9:g.124258258C>G NCBI36
NG_011554.1:g.52228C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1102C>G MANE Select ENSP00000357980.3:p.His368Asp
ENST00000648167.1:c.784C>G ENSP00000498033.1:p.His262Asp
ENST00000368984.7:c.1102C>G ENSP00000357980.3:p.His368Asp
ENST00000420892.1:c.325C>G ENSP00000412676.1:p.His109Asp
NM_002775.4:c.1102C>G NP_002766.1:p.His368Asp
NM_002775.5:c.1102C>G MANE Select NP_002766.1:p.His368Asp
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