Canonical Allele Identifier: CA1606874703
Gene: FAM50B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3836910_3836914delinsATAAT , CM000668.2:g.3836910_3836914delinsATAAT GRCh38
NC_000006.11:g.3837144_3837148delinsATAAT , CM000668.1:g.3837144_3837148delinsATAAT GRCh37
NC_000006.10:g.3782143_3782147delinsATAAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4899_-24+4903delinsATAAT XP_016866218.1:n.-24+4899_-24+4903delinsATAAT