Canonical Allele Identifier: CA1482797631
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542632G= , CM000666.2:g.105542632G= GRCh38
NC_000004.11:g.106463789G= , CM000666.1:g.106463789G= GRCh37
NC_000004.10:g.106683238G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.373C=
XR_939039.1:n.533C=
XR_939040.1:n.296-1156C=
XR_001741410.1:n.388C=
XR_001741411.1:n.864C=
XR_001741412.1:n.388C=
XR_001741413.1:n.388C=
XR_001741414.1:n.388C=
XR_939038.2:n.388C=
XR_939040.2:n.311-1156C=