Canonical Allele Identifier: CA1482797607
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542609A= , CM000666.2:g.105542609A= GRCh38
NC_000004.11:g.106463766A= , CM000666.1:g.106463766A= GRCh37
NC_000004.10:g.106683215A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.396T=
XR_939039.1:n.556T=
XR_939040.1:n.296-1133T=
XR_001741410.1:n.411T=
XR_001741411.1:n.887T=
XR_001741412.1:n.411T=
XR_001741413.1:n.411T=
XR_001741414.1:n.411T=
XR_939038.2:n.411T=
XR_939040.2:n.311-1133T=