Canonical Allele Identifier: CA64121848
Gene:

Linked Data

dbSNP Id: rs751206731

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.198767713G>C , CM000664.2:g.198767713G>C GRCh38
NC_000002.11:g.199632437G>C , CM000664.1:g.199632437G>C GRCh37
NC_000002.10:g.199340682G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923758.1:n.72+4546C>G
XR_923759.1:n.72+4546C>G
XR_923760.1:n.72+4546C>G
XR_923759.2:n.72+4546C>G
XR_923760.2:n.72+4546C>G