Canonical Allele Identifier: CA650482604
Gene: FAM50B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3836966G>A , CM000668.2:g.3836966G>A GRCh38
NC_000006.11:g.3837200G>A , CM000668.1:g.3837200G>A GRCh37
NC_000006.10:g.3782199G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4955G>A XP_016866218.1:n.-24+4955G>A