Canonical Allele Identifier: CA1678638482
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765643G= , CM000668.2:g.163765643G= GRCh38
NC_000006.11:g.164186675G= , CM000668.1:g.164186675G= GRCh37
NC_000006.10:g.164106665G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001744452.1:n.410+6214G=
XR_001744454.1:n.369+6255G=
XR_001744455.1:n.346+6278G=