Canonical Allele Identifier: CA216874337

Gene: BET1L

Linked Data

• dbSNP Id: rs1014387569
• gnomAD v2: 11-202778-C-T
• gnomAD v3: 11-202778-C-T
• gnomAD v4: 11-202778-C-T
• MyVariant Identifiers: chr11:g.202778C>T (hg19) ; chr11:g.202778C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.202778C>T , CM000673.2:g.202778C>T	GRCh38
NC_000011.9:g.202778C>T , CM000673.1:g.202778C>T	GRCh37
NC_000011.8:g.192778C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000410108.5:c.168+2833G>A	ENSP00000386558.1:n.168+2833G>A