Canonical Allele Identifier: CA11116955
Gene:

Linked Data

dbSNP Id: rs10211524
gnomAD v2: 2-65208074-G-A
gnomAD v3: 2-64980940-G-A
gnomAD v4: 2-64980940-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.64980940G>A , CM000664.2:g.64980940G>A GRCh38
NC_000002.11:g.65208074G>A , CM000664.1:g.65208074G>A GRCh37
NC_000002.10:g.65061578G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002959394.1:n.563-8901C>T
XR_002959395.1:n.622-8901C>T
XR_002959396.1:n.562-10155C>T
XR_002959397.1:n.303-8901C>T
XR_002959398.1:n.562-8901C>T
XR_002959399.1:n.559-24956C>T