Canonical Allele Identifier: CA660864959

Gene: HTRA1

Linked Data

• dbSNP Id: rs1370750796
• gnomAD v3: 10-122460974-A-G
• gnomAD v4: 10-122460974-A-G
• MyVariant Identifiers: chr10:g.124220490A>G (hg19) ; chr10:g.122460974A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122460974A>G , CM000672.2:g.122460974A>G	GRCh38
NC_000010.10:g.124220490A>G , CM000672.1:g.124220490A>G	GRCh37
NC_000010.9:g.124210480A>G	NCBI36
NG_011554.1:g.4450A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000648167.1:c.154+2265A>G	ENSP00000498033.1:n.154+2265A>G
XR_946382.1:n.385T>C
XR_946383.1:n.385T>C
XR_946384.1:n.385T>C
XR_946385.1:n.385T>C
XR_946382.2:n.413T>C
XR_946383.2:n.413T>C
XR_946384.2:n.389T>C
XR_946385.2:n.413T>C