Canonical Allele Identifier: CA1606874707
Gene: FAM50B HGNC NCBI

Linked Data

dbSNP Id: rs1581294702
gnomAD v3: 6-3836911-T-G
gnomAD v4: 6-3836911-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3836911T>G , CM000668.2:g.3836911T>G GRCh38
NC_000006.11:g.3837145T>G , CM000668.1:g.3837145T>G GRCh37
NC_000006.10:g.3782144T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4900T>G XP_016866218.1:n.-24+4900T>G