Canonical Allele Identifier: CA1482797561
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542584A= , CM000666.2:g.105542584A= GRCh38
NC_000004.11:g.106463741A= , CM000666.1:g.106463741A= GRCh37
NC_000004.10:g.106683190A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.421T=
XR_939039.1:n.581T=
XR_939040.1:n.296-1108T=
XR_001741410.1:n.436T=
XR_001741411.1:n.912T=
XR_001741412.1:n.436T=
XR_001741413.1:n.436T=
XR_001741414.1:n.436T=
XR_939038.2:n.436T=
XR_939040.2:n.311-1108T=