Canonical Allele Identifier: CA64121863
Gene:

Linked Data

dbSNP Id: rs570492585

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.198767749G>A , CM000664.2:g.198767749G>A GRCh38
NC_000002.11:g.199632473G>A , CM000664.1:g.199632473G>A GRCh37
NC_000002.10:g.199340718G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923758.1:n.72+4510C>T
XR_923759.1:n.72+4510C>T
XR_923760.1:n.72+4510C>T
XR_923759.2:n.72+4510C>T
XR_923760.2:n.72+4510C>T