Canonical Allele Identifier: CA308471504
Gene: CYP2B6 HGNC NCBI

Linked Data

dbSNP Id: rs574154609
gnomAD v2: 19-41524115-T-C
gnomAD v3: 19-41018210-T-C
gnomAD v4: 19-41018210-T-C
MyVariant Identifiers: chr19:g.41524115T>C (hg19) chr19:g.41018210T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41018210T>C , CM000681.2:g.41018210T>C GRCh38
NC_000019.9:g.41524115T>C , CM000681.1:g.41524115T>C GRCh37
NC_000019.8:g.46215955T>C NCBI36
NG_007929.1:g.31912T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.*1383T>C MANE Select ENSP00000324648.2:n.*1383T>C
ENST00000324071.8:c.*1383T>C ENSP00000324648.2:n.*1383T>C
NM_000767.4:c.*1383T>C NP_000758.1:n.*1383T>C
XM_011526548.1:c.*1383T>C XP_011524850.1:n.*1383T>C
XM_011526549.1:c.*1383T>C XP_011524851.1:n.*1383T>C
XM_011526550.1:c.*1383T>C XP_011524852.1:n.*1383T>C
NM_000767.5:c.*1383T>C MANE Select NP_000758.1:n.*1383T>C
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