Canonical Allele Identifier: CA1085457050
Gene: FAM50B HGNC NCBI

Linked Data

dbSNP Id: rs1761994500
gnomAD v3: 6-3837008-G-C
gnomAD v4: 6-3837008-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3837008G>C , CM000668.2:g.3837008G>C GRCh38
NC_000006.11:g.3837242G>C , CM000668.1:g.3837242G>C GRCh37
NC_000006.10:g.3782241G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4997G>C XP_016866218.1:n.-24+4997G>C