Canonical Allele Identifier: CA2749638106
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534678T>A , CM000664.2:g.41534678T>A GRCh38
NC_000002.11:g.41761818T>A , CM000664.1:g.41761818T>A GRCh37
NC_000002.10:g.41615322T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939996.1:n.181+3048A>T
XR_939997.1:n.146+3048A>T
XR_939997.2:n.9529+3048A>T