Canonical Allele Identifier: CA1482797542
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542561T= , CM000666.2:g.105542561T= GRCh38
NC_000004.11:g.106463718T= , CM000666.1:g.106463718T= GRCh37
NC_000004.10:g.106683167T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939038.1:n.444A=
XR_939039.1:n.604A=
XR_939040.1:n.296-1085A=
XR_001741410.1:n.459A=
XR_001741411.1:n.935A=
XR_001741412.1:n.449+10A=
XR_001741413.1:n.459A=
XR_001741414.1:n.449+10A=
XR_939038.2:n.459A=
XR_939040.2:n.311-1085A=