Canonical Allele Identifier: CA2753810660
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.198767691C>T , CM000664.2:g.198767691C>T GRCh38
NC_000002.11:g.199632415C>T , CM000664.1:g.199632415C>T GRCh37
NC_000002.10:g.199340660C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923758.1:n.72+4568G>A
XR_923759.1:n.72+4568G>A
XR_923760.1:n.72+4568G>A
XR_923759.2:n.72+4568G>A
XR_923760.2:n.72+4568G>A