Canonical Allele Identifier: CA1605276816
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465842A= , CM000668.2:g.465842A= GRCh38
NC_000006.11:g.465842A= , CM000668.1:g.465842A= GRCh37
NC_000006.10:g.410842A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12117A=
XR_926365.1:n.2548+12117A=
XR_001743914.1:n.482-9366A=