Canonical Allele Identifier: CA133776330

Gene: FAM50B

Linked Data

• dbSNP Id: rs555374958
• MyVariant Identifiers: chr6:g.3837239del (hg19) ; chr6:g.3837005del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.3837007del , CM000668.2:g.3837007del	GRCh38
NC_000006.11:g.3837241del , CM000668.1:g.3837241del	GRCh37
NC_000006.10:g.3782240del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017010729.1:c.-24+4996del	XP_016866218.1:n.-24+4996del