Canonical Allele Identifier: CA225652652
Gene:

Linked Data

dbSNP Id: rs11232369
gnomAD v2: 11-80562738-G-A
gnomAD v3: 11-80851695-G-A
gnomAD v4: 11-80851695-G-A
MyVariant Identifiers: chr11:g.80562738G>A (hg19) chr11:g.80851695G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.80851695G>A , CM000673.2:g.80851695G>A GRCh38
NC_000011.9:g.80562738G>A , CM000673.1:g.80562738G>A GRCh37
NC_000011.8:g.80240386G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247272.2:n.124+60596C>T
Search 100 bp 5'
Search 100 bp 3'