Canonical Allele Identifier: CA824452239

Gene: FAM50B

Linked Data

• dbSNP Id: rs1225910755
• gnomAD v3: 6-3836970-GC-G
• gnomAD v4: 6-3836970-GC-G
• MyVariant Identifiers: chr6:g.3837205del (hg19) ; chr6:g.3836971del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.3836971del , CM000668.2:g.3836971del	GRCh38
NC_000006.11:g.3837205del , CM000668.1:g.3837205del	GRCh37
NC_000006.10:g.3782204del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017010729.1:c.-24+4960del	XP_016866218.1:n.-24+4960del