Canonical Allele Identifier: CA1606874755
Gene: FAM50B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3837004_3837005delinsTA , CM000668.2:g.3837004_3837005delinsTA GRCh38
NC_000006.11:g.3837238_3837239delinsTA , CM000668.1:g.3837238_3837239delinsTA GRCh37
NC_000006.10:g.3782237_3782238delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4993_-24+4994delinsTA XP_016866218.1:n.-24+4993_-24+4994delinsTA