Canonical Allele Identifier: CA219000146
Gene:

Linked Data

dbSNP Id: rs10833583
gnomAD v2: 11-21669293-G-A
gnomAD v3: 11-21647747-G-A
gnomAD v4: 11-21647747-G-A
MyVariant Identifiers: chr11:g.21669293G>A (hg19) chr11:g.21647747G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.21647747G>A , CM000673.2:g.21647747G>A GRCh38
NC_000011.9:g.21669293G>A , CM000673.1:g.21669293G>A GRCh37
NC_000011.8:g.21625869G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001748150.1:n.585C>T
Search 100 bp 5'
Search 100 bp 3'