Canonical Allele Identifier: CA1482797526
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542546A= , CM000666.2:g.105542546A= GRCh38
NC_000004.11:g.106463703A= , CM000666.1:g.106463703A= GRCh37
NC_000004.10:g.106683152A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.459T=
XR_939039.1:n.619T=
XR_939040.1:n.296-1070T=
XR_001741410.1:n.474T=
XR_001741411.1:n.950T=
XR_001741412.1:n.449+25T=
XR_001741413.1:n.474T=
XR_001741414.1:n.449+25T=
XR_939038.2:n.474T=
XR_939040.2:n.311-1070T=