Canonical Allele Identifier: CA1112576822
Gene:

Linked Data

dbSNP Id: rs1802340286
gnomAD v3: 8-33808166-C-A
gnomAD v4: 8-33808166-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.33808166C>A , CM000670.2:g.33808166C>A GRCh38
NC_000008.10:g.33665684C>A , CM000670.1:g.33665684C>A GRCh37
NC_000008.9:g.33785226C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949659.1:n.240+11730C>A
XR_002956701.1:n.240+11730C>A