Canonical Allele Identifier: CA473651108
Gene:

Linked Data

dbSNP Id: rs1366136087
gnomAD v2: 11-27505631-G-A
gnomAD v3: 11-27484084-G-A
gnomAD v4: 11-27484084-G-A
MyVariant Identifiers: chr11:g.27505631G>A (hg19) chr11:g.27484084G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484084G>A , CM000673.2:g.27484084G>A GRCh38
NC_000011.9:g.27505631G>A , CM000673.1:g.27505631G>A GRCh37
NC_000011.8:g.27462207G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.235G>A
Search 100 bp 5'
Search 100 bp 3'