Canonical Allele Identifier: CA1678638472
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765618C= , CM000668.2:g.163765618C= GRCh38
NC_000006.11:g.164186650C= , CM000668.1:g.164186650C= GRCh37
NC_000006.10:g.164106640C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001744452.1:n.410+6189C=
XR_001744454.1:n.369+6230C=
XR_001744455.1:n.346+6253C=