Canonical Allele Identifier: CA1606874687
Gene: FAM50B HGNC NCBI

Linked Data

dbSNP Id: rs1761992260

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3836868A>G , CM000668.2:g.3836868A>G GRCh38
NC_000006.11:g.3837102A>G , CM000668.1:g.3837102A>G GRCh37
NC_000006.10:g.3782101A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4857A>G XP_016866218.1:n.-24+4857A>G