Canonical Allele Identifier: CA1606874692
Gene: FAM50B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3836877T= , CM000668.2:g.3836877T= GRCh38
NC_000006.11:g.3837111T= , CM000668.1:g.3837111T= GRCh37
NC_000006.10:g.3782110T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4866T= XP_016866218.1:n.-24+4866T=