Canonical Allele Identifier: CA133776317

Gene: FAM50B

Linked Data

• dbSNP Id: rs1050076420
• gnomAD v3: 6-3836883-A-C
• gnomAD v4: 6-3836883-A-C
• MyVariant Identifiers: chr6:g.3837117A>C (hg19) ; chr6:g.3836883A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.3836883A>C , CM000668.2:g.3836883A>C	GRCh38
NC_000006.11:g.3837117A>C , CM000668.1:g.3837117A>C	GRCh37
NC_000006.10:g.3782116A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017010729.1:c.-24+4872A>C	XP_016866218.1:n.-24+4872A>C