Canonical Allele Identifier: CA5725959
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs202171123
ExAC: 10:124266311 C / T
gnomAD v2: 10-124266311-C-T
gnomAD v3: 10-122506795-C-T
gnomAD v4: 10-122506795-C-T
MyVariant Identifiers: chr10:g.124266311C>T (hg19) chr10:g.122506795C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506795C>T , CM000672.2:g.122506795C>T GRCh38
NC_000010.10:g.124266311C>T , CM000672.1:g.124266311C>T GRCh37
NC_000010.9:g.124256301C>T NCBI36
NG_011554.1:g.50271C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.882C>T MANE Select ENSP00000357980.3:p.Thr294=
ENST00000648167.1:c.564C>T ENSP00000498033.1:p.Thr188=
ENST00000368984.7:c.882C>T ENSP00000357980.3:p.Thr294=
ENST00000420892.1:c.105C>T ENSP00000412676.1:p.Thr35=
NM_002775.4:c.882C>T NP_002766.1:p.Thr294=
NM_002775.5:c.882C>T MANE Select NP_002766.1:p.Thr294=
Search 100 bp 5'
Search 100 bp 3'