Canonical Allele Identifier: CA1482797602
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542604G= , CM000666.2:g.105542604G= GRCh38
NC_000004.11:g.106463761G= , CM000666.1:g.106463761G= GRCh37
NC_000004.10:g.106683210G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.401C=
XR_939039.1:n.561C=
XR_939040.1:n.296-1128C=
XR_001741410.1:n.416C=
XR_001741411.1:n.892C=
XR_001741412.1:n.416C=
XR_001741413.1:n.416C=
XR_001741414.1:n.416C=
XR_939038.2:n.416C=
XR_939040.2:n.311-1128C=