Canonical Allele Identifier: CA2671644299
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542533C>A , CM000666.2:g.105542533C>A GRCh38
NC_000004.11:g.106463690C>A , CM000666.1:g.106463690C>A GRCh37
NC_000004.10:g.106683139C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.472G>T
XR_939039.1:n.632G>T
XR_939040.1:n.296-1057G>T
XR_001741410.1:n.487G>T
XR_001741411.1:n.963G>T
XR_001741412.1:n.449+38G>T
XR_001741413.1:n.487G>T
XR_001741414.1:n.449+38G>T
XR_939038.2:n.487G>T
XR_939040.2:n.311-1057G>T