Canonical Allele Identifier: CA216874420
Gene: BET1L HGNC NCBI

Linked Data

dbSNP Id: rs184433312
gnomAD v3: 11-202905-G-A
gnomAD v4: 11-202905-G-A
MyVariant Identifiers: chr11:g.202905G>A (hg19) chr11:g.202905G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.202905G>A , CM000673.2:g.202905G>A GRCh38
NC_000011.9:g.202905G>A , CM000673.1:g.202905G>A GRCh37
NC_000011.8:g.192905G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000410108.5:c.168+2706C>T ENSP00000386558.1:n.168+2706C>T
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