Canonical Allele Identifier: CA1482797500
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542518T= , CM000666.2:g.105542518T= GRCh38
NC_000004.11:g.106463675T= , CM000666.1:g.106463675T= GRCh37
NC_000004.10:g.106683124T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.487A=
XR_939039.1:n.647A=
XR_939040.1:n.296-1042A=
XR_001741410.1:n.502A=
XR_001741411.1:n.978A=
XR_001741412.1:n.449+53A=
XR_001741413.1:n.502A=
XR_001741414.1:n.449+53A=
XR_939038.2:n.502A=
XR_939040.2:n.311-1042A=