Canonical Allele Identifier: CA2499816089
Gene: FAM50B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3836982T>C , CM000668.2:g.3836982T>C GRCh38
NC_000006.11:g.3837216T>C , CM000668.1:g.3837216T>C GRCh37
NC_000006.10:g.3782215T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4971T>C XP_016866218.1:n.-24+4971T>C