Canonical Allele Identifier: CA824452225

Gene: FAM50B

Linked Data

• dbSNP Id: rs1208089111
• gnomAD v3: 6-3836963-CG-C
• gnomAD v4: 6-3836963-CG-C
• MyVariant Identifiers: chr6:g.3837198del (hg19) ; chr6:g.3836964del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.3836964del , CM000668.2:g.3836964del	GRCh38
NC_000006.11:g.3837198del , CM000668.1:g.3837198del	GRCh37
NC_000006.10:g.3782197del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017010729.1:c.-24+4953del	XP_016866218.1:n.-24+4953del