Canonical Allele Identifier: CA2749638114
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534736C>A , CM000664.2:g.41534736C>A GRCh38
NC_000002.11:g.41761876C>A , CM000664.1:g.41761876C>A GRCh37
NC_000002.10:g.41615380C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+2990G>T
XR_939997.1:n.146+2990G>T
XR_939997.2:n.9529+2990G>T