Canonical Allele Identifier: CA1606874765
Gene: FAM50B HGNC NCBI

Linked Data

dbSNP Id: rs1761994607

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3837026A>C , CM000668.2:g.3837026A>C GRCh38
NC_000006.11:g.3837260A>C , CM000668.1:g.3837260A>C GRCh37
NC_000006.10:g.3782259A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+5015A>C XP_016866218.1:n.-24+5015A>C