Canonical Allele Identifier: CA2671644296
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542501C>A , CM000666.2:g.105542501C>A GRCh38
NC_000004.11:g.106463658C>A , CM000666.1:g.106463658C>A GRCh37
NC_000004.10:g.106683107C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.504G>T
XR_939039.1:n.664G>T
XR_939040.1:n.296-1025G>T
XR_001741410.1:n.519G>T
XR_001741411.1:n.995G>T
XR_001741412.1:n.449+70G>T
XR_001741413.1:n.519G>T
XR_001741414.1:n.449+70G>T
XR_939038.2:n.519G>T
XR_939040.2:n.311-1025G>T