Canonical Allele Identifier: CA136521675
Gene:

Linked Data

dbSNP Id: rs7771911
gnomAD v2: 6-23437676-C-A
gnomAD v3: 6-23437448-C-A
gnomAD v4: 6-23437448-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.23437448C>A , CM000668.2:g.23437448C>A GRCh38
NC_000006.11:g.23437676C>A , CM000668.1:g.23437676C>A GRCh37
NC_000006.10:g.23545655C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926586.1:n.174-4132C>A
XR_926600.1:n.359+20142G>T
XR_926601.1:n.359+20142G>T
XR_001744046.1:n.481+20142G>T
XR_001744048.1:n.792-4132C>A