Canonical Allele Identifier: CA1606874704
Gene: FAM50B HGNC NCBI

Linked Data

dbSNP Id: rs1761992582

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3836911_3836914del , CM000668.2:g.3836911_3836914del GRCh38
NC_000006.11:g.3837145_3837148del , CM000668.1:g.3837145_3837148del GRCh37
NC_000006.10:g.3782144_3782147del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4900_-24+4903del XP_016866218.1:n.-24+4900_-24+4903del