Canonical Allele Identifier: CA1665449762
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134398840C= , CM000668.2:g.134398840C= GRCh38
NC_000006.11:g.134719978C= , CM000668.1:g.134719978C= GRCh37
NC_000006.10:g.134761671C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428023.2:n.23+111C=