Canonical Allele Identifier: CA596578950
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1182189240
gnomAD v2: 10-124221022-C-T
gnomAD v3: 10-122461506-C-T
gnomAD v4: 10-122461506-C-T
MyVariant Identifiers: chr10:g.124221022C>T (hg19) chr10:g.122461506C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461506C>T , CM000672.2:g.122461506C>T GRCh38
NC_000010.10:g.124221022C>T , CM000672.1:g.124221022C>T GRCh37
NC_000010.9:g.124211012C>T NCBI36
NG_011554.1:g.4982C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648167.1:c.154+2797C>T ENSP00000498033.1:n.154+2797C>T
Search 100 bp 5'
Search 100 bp 3'