Canonical Allele Identifier: CA12843940
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.101215695A>C , CM000670.2:g.101215695A>C GRCh38
NC_000008.10:g.102227923A>C , CM000670.1:g.102227923A>C GRCh37
NC_000008.9:g.102297099A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011517414.1:c.-277+1270A>C XP_011515716.1:n.-277+1270A>C
XM_011517415.1:c.-41+1270A>C XP_011515717.1:n.-41+1270A>C
XM_011517417.1:c.-54+1270A>C XP_011515719.1:n.-54+1270A>C
XR_928468.1:n.395+1270A>C
XR_928469.1:n.395+1270A>C
XR_928468.2:n.667+1270A>C
XR_928469.2:n.667+1270A>C