Canonical Allele Identifier: CA473651094
Gene:

Linked Data

dbSNP Id: rs1422515314
gnomAD v4: 11-27484079-G-A
MyVariant Identifiers: chr11:g.27505626G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484079G>A , CM000673.2:g.27484079G>A GRCh38
NC_000011.9:g.27505626G>A , CM000673.1:g.27505626G>A GRCh37
NC_000011.8:g.27462202G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.230G>A
Search 100 bp 5'
Search 100 bp 3'