Canonical Allele Identifier: CA1606874754
Gene: FAM50B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3837001A= , CM000668.2:g.3837001A= GRCh38
NC_000006.11:g.3837235A= , CM000668.1:g.3837235A= GRCh37
NC_000006.10:g.3782234A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4990A= XP_016866218.1:n.-24+4990A=