Canonical Allele Identifier: CA214414667

Gene: HTRA1

Linked Data

• dbSNP Id: rs1035648199
• gnomAD v2: 10-124220613-G-A
• gnomAD v3: 10-122461097-G-A
• gnomAD v4: 10-122461097-G-A
• MyVariant Identifiers: chr10:g.124220613G>A (hg19) ; chr10:g.122461097G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122461097G>A , CM000672.2:g.122461097G>A	GRCh38
NC_000010.10:g.124220613G>A , CM000672.1:g.124220613G>A	GRCh37
NC_000010.9:g.124210603G>A	NCBI36
NG_011554.1:g.4573G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648167.1:c.154+2388G>A	ENSP00000498033.1:n.154+2388G>A
XR_946382.1:n.262C>T
XR_946383.1:n.262C>T
XR_946384.1:n.262C>T
XR_946385.1:n.262C>T
XR_946382.2:n.290C>T
XR_946383.2:n.290C>T
XR_946384.2:n.266C>T
XR_946385.2:n.290C>T