Canonical Allele Identifier: CA133776326

Gene: FAM50B

Linked Data

• dbSNP Id: rs993656519
• gnomAD v3: 6-3836972-T-A
• gnomAD v4: 6-3836972-T-A
• MyVariant Identifiers: chr6:g.3837206T>A (hg19) ; chr6:g.3836972T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.3836972T>A , CM000668.2:g.3836972T>A	GRCh38
NC_000006.11:g.3837206T>A , CM000668.1:g.3837206T>A	GRCh37
NC_000006.10:g.3782205T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017010729.1:c.-24+4961T>A	XP_016866218.1:n.-24+4961T>A