Canonical Allele Identifier: CA1605276805
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465823T= , CM000668.2:g.465823T= GRCh38
NC_000006.11:g.465823T= , CM000668.1:g.465823T= GRCh37
NC_000006.10:g.410823T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12098T=
XR_926365.1:n.2548+12098T=
XR_001743914.1:n.482-9385T=