Canonical Allele Identifier: CA1665604349
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134773170C= , CM000668.2:g.134773170C= GRCh38
NC_000006.11:g.135094308C= , CM000668.1:g.135094308C= GRCh37
NC_000006.10:g.135136001C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943008.1:n.368+32568G=
XR_943009.1:n.368+32568G=
XR_001744363.1:n.414+32568G=
XR_001744364.1:n.342+32568G=