Canonical Allele Identifier: CA995933588
Gene: CYP2B6 HGNC NCBI

Linked Data

dbSNP Id: rs1969404017
gnomAD v3: 19-41018392-A-G
gnomAD v4: 19-41018392-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41018392A>G , CM000681.2:g.41018392A>G GRCh38
NC_000019.9:g.41524297A>G , CM000681.1:g.41524297A>G GRCh37
NC_000019.8:g.46216137A>G NCBI36
NG_007929.1:g.32094A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.*1565A>G MANE Select ENSP00000324648.2:n.*1565A>G
ENST00000324071.8:c.*1565A>G ENSP00000324648.2:n.*1565A>G
NM_000767.4:c.*1565A>G NP_000758.1:n.*1565A>G
XM_011526548.1:c.*1565A>G XP_011524850.1:n.*1565A>G
XM_011526549.1:c.*1565A>G XP_011524851.1:n.*1565A>G
XM_011526550.1:c.*1565A>G XP_011524852.1:n.*1565A>G
NM_000767.5:c.*1565A>G MANE Select NP_000758.1:n.*1565A>G
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