Canonical Allele Identifier: CA133776331

Gene: FAM50B

Linked Data

• dbSNP Id: rs551242729
• MyVariant Identifiers: chr6:g.3837263A>T (hg19) ; chr6:g.3837029A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.3837029A>T , CM000668.2:g.3837029A>T	GRCh38
NC_000006.11:g.3837263A>T , CM000668.1:g.3837263A>T	GRCh37
NC_000006.10:g.3782262A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017010729.1:c.-24+5018A>T	XP_016866218.1:n.-24+5018A>T