Canonical Allele Identifier: CA1085457046

Gene: FAM50B

Linked Data

• dbSNP Id: rs1761993373
• gnomAD v3: 6-3836967-C-A
• gnomAD v4: 6-3836967-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.3836967C>A , CM000668.2:g.3836967C>A	GRCh38
NC_000006.11:g.3837201C>A , CM000668.1:g.3837201C>A	GRCh37
NC_000006.10:g.3782200C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017010729.1:c.-24+4956C>A	XP_016866218.1:n.-24+4956C>A