Canonical Allele Identifier: CA824452242

Gene: FAM50B

Linked Data

• dbSNP Id: rs1445668117
• MyVariant Identifiers: chr6:g.3837218T>C (hg19) ; chr6:g.3836984T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.3836984T>C , CM000668.2:g.3836984T>C	GRCh38
NC_000006.11:g.3837218T>C , CM000668.1:g.3837218T>C	GRCh37
NC_000006.10:g.3782217T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017010729.1:c.-24+4973T>C	XP_016866218.1:n.-24+4973T>C