Canonical Allele Identifier: CA674443385
Gene: BET1L HGNC NCBI

Linked Data

dbSNP Id: rs1412402868
gnomAD v3: 11-202910-C-T
gnomAD v4: 11-202910-C-T
MyVariant Identifiers: chr11:g.202910C>T (hg19) chr11:g.202910C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.202910C>T , CM000673.2:g.202910C>T GRCh38
NC_000011.9:g.202910C>T , CM000673.1:g.202910C>T GRCh37
NC_000011.8:g.192910C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000410108.5:c.168+2701G>A ENSP00000386558.1:n.168+2701G>A
Search 100 bp 5'
Search 100 bp 3'