Canonical Allele Identifier: CA5725775
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs775063870
ExAC: 10:124221055 G / C
gnomAD v2: 10-124221055-G-C
gnomAD v3: 10-122461539-G-C
gnomAD v4: 10-122461539-G-C
MyVariant Identifiers: chr10:g.124221055G>C (hg19) chr10:g.122461539G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461539G>C , CM000672.2:g.122461539G>C GRCh38
NC_000010.10:g.124221055G>C , CM000672.1:g.124221055G>C GRCh37
NC_000010.9:g.124211045G>C NCBI36
NG_011554.1:g.5015G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648167.1:c.154+2830G>C ENSP00000498033.1:n.154+2830G>C
ENST00000368984.7:c.-114G>C ENSP00000357980.3:n.-114G>C
NM_002775.4:c.-114G>C NP_002766.1:n.-114G>C
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