Canonical Allele Identifier: CA914362333
Gene:

Linked Data

dbSNP Id: rs1558371332
gnomAD v2: 2-16639535-A-T
gnomAD v3: 2-16458267-A-T
gnomAD v4: 2-16458267-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458267A>T , CM000664.2:g.16458267A>T GRCh38
NC_000002.11:g.16639535A>T , CM000664.1:g.16639535A>T GRCh37
NC_000002.10:g.16503016A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939752.1:n.396-3173T>A