Canonical Allele Identifier: CA1665604328
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134773143C= , CM000668.2:g.134773143C= GRCh38
NC_000006.11:g.135094281C= , CM000668.1:g.135094281C= GRCh37
NC_000006.10:g.135135974C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943008.1:n.368+32595G=
XR_943009.1:n.368+32595G=
XR_001744363.1:n.414+32595G=
XR_001744364.1:n.342+32595G=