Canonical Allele Identifier: CA674443389
Gene: BET1L HGNC NCBI

Linked Data

dbSNP Id: rs1184766386
gnomAD v3: 11-202921-T-G
gnomAD v4: 11-202921-T-G
MyVariant Identifiers: chr11:g.202921T>G (hg19) chr11:g.202921T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.202921T>G , CM000673.2:g.202921T>G GRCh38
NC_000011.9:g.202921T>G , CM000673.1:g.202921T>G GRCh37
NC_000011.8:g.192921T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000410108.5:c.168+2690A>C ENSP00000386558.1:n.168+2690A>C
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