Canonical Allele Identifier: CA1482797453
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542482T= , CM000666.2:g.105542482T= GRCh38
NC_000004.11:g.106463639T= , CM000666.1:g.106463639T= GRCh37
NC_000004.10:g.106683088T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.523A=
XR_939039.1:n.683A=
XR_939040.1:n.296-1006A=
XR_001741410.1:n.538A=
XR_001741411.1:n.1014A=
XR_001741412.1:n.449+89A=
XR_001741413.1:n.538A=
XR_001741414.1:n.449+89A=
XR_939038.2:n.538A=
XR_939040.2:n.311-1006A=