Canonical Allele Identifier: CA1482797505
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542526G= , CM000666.2:g.105542526G= GRCh38
NC_000004.11:g.106463683G= , CM000666.1:g.106463683G= GRCh37
NC_000004.10:g.106683132G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.479C=
XR_939039.1:n.639C=
XR_939040.1:n.296-1050C=
XR_001741410.1:n.494C=
XR_001741411.1:n.970C=
XR_001741412.1:n.449+45C=
XR_001741413.1:n.494C=
XR_001741414.1:n.449+45C=
XR_939038.2:n.494C=
XR_939040.2:n.311-1050C=