Canonical Allele Identifier: CA214411692
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs770347880
gnomAD v2: 10-124266781-T-C
gnomAD v3: 10-122507265-T-C
gnomAD v4: 10-122507265-T-C
MyVariant Identifiers: chr10:g.124266781T>C (hg19) chr10:g.122507265T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122507265T>C , CM000672.2:g.122507265T>C GRCh38
NC_000010.10:g.124266781T>C , CM000672.1:g.124266781T>C GRCh37
NC_000010.9:g.124256771T>C NCBI36
NG_011554.1:g.50741T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.973-105T>C MANE Select ENSP00000357980.3:n.973-105T>C
ENST00000648167.1:c.655-105T>C ENSP00000498033.1:n.655-105T>C
ENST00000368984.7:c.973-105T>C ENSP00000357980.3:n.973-105T>C
ENST00000420892.1:c.196-105T>C ENSP00000412676.1:n.196-105T>C
NM_002775.4:c.973-105T>C NP_002766.1:n.973-105T>C
NM_002775.5:c.973-105T>C MANE Select NP_002766.1:n.973-105T>C
Search 100 bp 5'
Search 100 bp 3'