Canonical Allele Identifier: CA1482798059
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542970G= , CM000666.2:g.105542970G= GRCh38
NC_000004.11:g.106464127G= , CM000666.1:g.106464127G= GRCh37
NC_000004.10:g.106683576G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-261C=
XR_939039.1:n.456-261C=
XR_939040.1:n.296-1494C=
XR_001741410.1:n.311-261C=
XR_001741411.1:n.787-261C=
XR_001741412.1:n.311-261C=
XR_001741413.1:n.311-261C=
XR_001741414.1:n.311-261C=
XR_939038.2:n.311-261C=
XR_939040.2:n.311-1494C=