Canonical Allele Identifier: CA1606874713
Gene: FAM50B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3836916C= , CM000668.2:g.3836916C= GRCh38
NC_000006.11:g.3837150C= , CM000668.1:g.3837150C= GRCh37
NC_000006.10:g.3782149C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4905C= XP_016866218.1:n.-24+4905C=