Canonical Allele Identifier: CA214414969
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1011242095
gnomAD v4: 10-122461500-A-G
MyVariant Identifiers: chr10:g.124221016A>G (hg19) chr10:g.122461500A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461500A>G , CM000672.2:g.122461500A>G GRCh38
NC_000010.10:g.124221016A>G , CM000672.1:g.124221016A>G GRCh37
NC_000010.9:g.124211006A>G NCBI36
NG_011554.1:g.4976A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648167.1:c.154+2791A>G ENSP00000498033.1:n.154+2791A>G
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