Canonical Allele Identifier: CA11659343
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.124160218G>A , CM000666.2:g.124160218G>A GRCh38
NC_000004.11:g.125081373G>A , CM000666.1:g.125081373G>A GRCh37
NC_000004.10:g.125300823G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939176.1:n.114+27926C>T
XR_939177.1:n.114+27926C>T
XR_939176.2:n.277+27926C>T
XR_939177.2:n.277+27926C>T