Canonical Allele Identifier: CA1482797670
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542654T= , CM000666.2:g.105542654T= GRCh38
NC_000004.11:g.106463811T= , CM000666.1:g.106463811T= GRCh37
NC_000004.10:g.106683260T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.351A=
XR_939039.1:n.511A=
XR_939040.1:n.296-1178A=
XR_001741410.1:n.366A=
XR_001741411.1:n.842A=
XR_001741412.1:n.366A=
XR_001741413.1:n.366A=
XR_001741414.1:n.366A=
XR_939038.2:n.366A=
XR_939040.2:n.311-1178A=