Canonical Allele Identifier: CA2710773999
Gene: FAM50B HGNC NCBI

Linked Data

dbSNP Id: rs1375095556

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3836867C>G , CM000668.2:g.3836867C>G GRCh38
NC_000006.11:g.3837101C>G , CM000668.1:g.3837101C>G GRCh37
NC_000006.10:g.3782100C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4856C>G XP_016866218.1:n.-24+4856C>G