Canonical Allele Identifier: CA1605276831
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465867G= , CM000668.2:g.465867G= GRCh38
NC_000006.11:g.465867G= , CM000668.1:g.465867G= GRCh37
NC_000006.10:g.410867G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12142G=
XR_926365.1:n.2548+12142G=
XR_001743914.1:n.482-9341G=