Canonical Allele Identifier: CA1482797495
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542507C= , CM000666.2:g.105542507C= GRCh38
NC_000004.11:g.106463664C= , CM000666.1:g.106463664C= GRCh37
NC_000004.10:g.106683113C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939038.1:n.498G=
XR_939039.1:n.658G=
XR_939040.1:n.296-1031G=
XR_001741410.1:n.513G=
XR_001741411.1:n.989G=
XR_001741412.1:n.449+64G=
XR_001741413.1:n.513G=
XR_001741414.1:n.449+64G=
XR_939038.2:n.513G=
XR_939040.2:n.311-1031G=