Canonical Allele Identifier: CA1482797520
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542535A= , CM000666.2:g.105542535A= GRCh38
NC_000004.11:g.106463692A= , CM000666.1:g.106463692A= GRCh37
NC_000004.10:g.106683141A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.470T=
XR_939039.1:n.630T=
XR_939040.1:n.296-1059T=
XR_001741410.1:n.485T=
XR_001741411.1:n.961T=
XR_001741412.1:n.449+36T=
XR_001741413.1:n.485T=
XR_001741414.1:n.449+36T=
XR_939038.2:n.485T=
XR_939040.2:n.311-1059T=