Canonical Allele Identifier: CA1606874767
Gene: FAM50B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3837035A= , CM000668.2:g.3837035A= GRCh38
NC_000006.11:g.3837269A= , CM000668.1:g.3837269A= GRCh37
NC_000006.10:g.3782268A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+5024A= XP_016866218.1:n.-24+5024A=