Canonical Allele Identifier: CA1678638489
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765649G= , CM000668.2:g.163765649G= GRCh38
NC_000006.11:g.164186681G= , CM000668.1:g.164186681G= GRCh37
NC_000006.10:g.164106671G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6220G=
XR_001744454.1:n.369+6261G=
XR_001744455.1:n.346+6284G=