Canonical Allele Identifier: CA1482797640
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542635C= , CM000666.2:g.105542635C= GRCh38
NC_000004.11:g.106463792C= , CM000666.1:g.106463792C= GRCh37
NC_000004.10:g.106683241C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.370G=
XR_939039.1:n.530G=
XR_939040.1:n.296-1159G=
XR_001741410.1:n.385G=
XR_001741411.1:n.861G=
XR_001741412.1:n.385G=
XR_001741413.1:n.385G=
XR_001741414.1:n.385G=
XR_939038.2:n.385G=
XR_939040.2:n.311-1159G=