Canonical Allele Identifier: CA1606874745
Gene: FAM50B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3836970_3836971delinsGC , CM000668.2:g.3836970_3836971delinsGC GRCh38
NC_000006.11:g.3837204_3837205delinsGC , CM000668.1:g.3837204_3837205delinsGC GRCh37
NC_000006.10:g.3782203_3782204delinsGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4959_-24+4960delinsGC XP_016866218.1:n.-24+4959_-24+4960delinsGC
Search 100 bp 5'
Search 100 bp 3'