Canonical Allele Identifier: CA650482609
Gene: FAM50B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3837038G>A , CM000668.2:g.3837038G>A GRCh38
NC_000006.11:g.3837272G>A , CM000668.1:g.3837272G>A GRCh37
NC_000006.10:g.3782271G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+5027G>A XP_016866218.1:n.-24+5027G>A