Canonical Allele Identifier: CA64121889
Gene:

Linked Data

dbSNP Id: rs962466440

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.198767881A>T , CM000664.2:g.198767881A>T GRCh38
NC_000002.11:g.199632605A>T , CM000664.1:g.199632605A>T GRCh37
NC_000002.10:g.199340850A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923758.1:n.72+4378T>A
XR_923759.1:n.72+4378T>A
XR_923760.1:n.72+4378T>A
XR_923759.2:n.72+4378T>A
XR_923760.2:n.72+4378T>A