Canonical Allele Identifier: CA5725928

Gene: HTRA1

Linked Data

• dbSNP Id: rs765778614
• ExAC: 10:124266198 T / C
• gnomAD v2: 10-124266198-T-C
• gnomAD v3: 10-122506682-T-C
• gnomAD v4: 10-122506682-T-C
• MyVariant Identifiers: chr10:g.124266198T>C (hg19) ; chr10:g.122506682T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122506682T>C , CM000672.2:g.122506682T>C	GRCh38
NC_000010.10:g.124266198T>C , CM000672.1:g.124266198T>C	GRCh37
NC_000010.9:g.124256188T>C	NCBI36
NG_011554.1:g.50158T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368984.8:c.778-9T>C MANE Select	ENSP00000357980.3:n.778-9T>C
ENST00000648167.1:c.460-9T>C	ENSP00000498033.1:n.460-9T>C
ENST00000368984.7:c.778-9T>C	ENSP00000357980.3:n.778-9T>C
NM_002775.4:c.778-9T>C	NP_002766.1:n.778-9T>C
NM_002775.5:c.778-9T>C MANE Select	NP_002766.1:n.778-9T>C