Canonical Allele Identifier: CA214414760
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs983306594
gnomAD v3: 10-122461180-C-T
gnomAD v4: 10-122461180-C-T
MyVariant Identifiers: chr10:g.124220696C>T (hg19) chr10:g.122461180C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461180C>T , CM000672.2:g.122461180C>T GRCh38
NC_000010.10:g.124220696C>T , CM000672.1:g.124220696C>T GRCh37
NC_000010.9:g.124210686C>T NCBI36
NG_011554.1:g.4656C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000648167.1:c.154+2471C>T ENSP00000498033.1:n.154+2471C>T
XR_946382.1:n.179G>A
XR_946383.1:n.179G>A
XR_946384.1:n.179G>A
XR_946385.1:n.179G>A
XR_946382.2:n.207G>A
XR_946383.2:n.207G>A
XR_946384.2:n.183G>A
XR_946385.2:n.207G>A
Search 100 bp 5'
Search 100 bp 3'