Canonical Allele Identifier: CA1482797487
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542501C= , CM000666.2:g.105542501C= GRCh38
NC_000004.11:g.106463658C= , CM000666.1:g.106463658C= GRCh37
NC_000004.10:g.106683107C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.504G=
XR_939039.1:n.664G=
XR_939040.1:n.296-1025G=
XR_001741410.1:n.519G=
XR_001741411.1:n.995G=
XR_001741412.1:n.449+70G=
XR_001741413.1:n.519G=
XR_001741414.1:n.449+70G=
XR_939038.2:n.519G=
XR_939040.2:n.311-1025G=