Canonical Allele Identifier: CA1482797929
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542861A= , CM000666.2:g.105542861A= GRCh38
NC_000004.11:g.106464018A= , CM000666.1:g.106464018A= GRCh37
NC_000004.10:g.106683467A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-152T=
XR_939039.1:n.456-152T=
XR_939040.1:n.296-1385T=
XR_001741410.1:n.311-152T=
XR_001741411.1:n.787-152T=
XR_001741412.1:n.311-152T=
XR_001741413.1:n.311-152T=
XR_001741414.1:n.311-152T=
XR_939038.2:n.311-152T=
XR_939040.2:n.311-1385T=