Canonical Allele Identifier: CA1085457040
Gene: FAM50B HGNC NCBI

Linked Data

dbSNP Id: rs1761992397
gnomAD v3: 6-3836878-C-T
gnomAD v4: 6-3836878-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3836878C>T , CM000668.2:g.3836878C>T GRCh38
NC_000006.11:g.3837112C>T , CM000668.1:g.3837112C>T GRCh37
NC_000006.10:g.3782111C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4867C>T XP_016866218.1:n.-24+4867C>T