Canonical Allele Identifier: CA64121882
Gene:

Linked Data

dbSNP Id: rs989854488

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.198767863A>G , CM000664.2:g.198767863A>G GRCh38
NC_000002.11:g.199632587A>G , CM000664.1:g.199632587A>G GRCh37
NC_000002.10:g.199340832A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923758.1:n.72+4396T>C
XR_923759.1:n.72+4396T>C
XR_923760.1:n.72+4396T>C
XR_923759.2:n.72+4396T>C
XR_923760.2:n.72+4396T>C