Canonical Allele Identifier: CA1029770044
Gene:

Linked Data

dbSNP Id: rs1667992498
gnomAD v3: 2-41534742-C-A
gnomAD v4: 2-41534742-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534742C>A , CM000664.2:g.41534742C>A GRCh38
NC_000002.11:g.41761882C>A , CM000664.1:g.41761882C>A GRCh37
NC_000002.10:g.41615386C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939996.1:n.181+2984G>T
XR_939997.1:n.146+2984G>T
XR_939997.2:n.9529+2984G>T