Canonical Allele Identifier: CA660865174
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1038348682
gnomAD v3: 10-122461211-G-C
gnomAD v4: 10-122461211-G-C
MyVariant Identifiers: chr10:g.124220727G>C (hg19) chr10:g.122461211G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461211G>C , CM000672.2:g.122461211G>C GRCh38
NC_000010.10:g.124220727G>C , CM000672.1:g.124220727G>C GRCh37
NC_000010.9:g.124210717G>C NCBI36
NG_011554.1:g.4687G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648167.1:c.154+2502G>C ENSP00000498033.1:n.154+2502G>C
XR_946382.1:n.148C>G
XR_946383.1:n.148C>G
XR_946384.1:n.148C>G
XR_946385.1:n.148C>G
XR_946382.2:n.176C>G
XR_946383.2:n.176C>G
XR_946384.2:n.152C>G
XR_946385.2:n.176C>G
Search 100 bp 5'
Search 100 bp 3'