Canonical Allele Identifier: CA1606874741
Gene: FAM50B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3836963_3836964delinsCG , CM000668.2:g.3836963_3836964delinsCG GRCh38
NC_000006.11:g.3837197_3837198delinsCG , CM000668.1:g.3837197_3837198delinsCG GRCh37
NC_000006.10:g.3782196_3782197delinsCG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4952_-24+4953delinsCG XP_016866218.1:n.-24+4952_-24+4953delinsCG
Search 100 bp 5'
Search 100 bp 3'