Canonical Allele Identifier: CA1482797442
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542466C= , CM000666.2:g.105542466C= GRCh38
NC_000004.11:g.106463623C= , CM000666.1:g.106463623C= GRCh37
NC_000004.10:g.106683072C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.539G=
XR_939039.1:n.699G=
XR_939040.1:n.296-990G=
XR_001741410.1:n.554G=
XR_001741411.1:n.1030G=
XR_001741412.1:n.449+105G=
XR_001741413.1:n.554G=
XR_001741414.1:n.449+105G=
XR_939038.2:n.554G=
XR_939040.2:n.311-990G=