Canonical Allele Identifier: CA308471359
Gene: CYP2B6 HGNC NCBI

Linked Data

dbSNP Id: rs557071267
MyVariant Identifiers: chr19:g.41523998C>A (hg19) chr19:g.41018093C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41018093C>A , CM000681.2:g.41018093C>A GRCh38
NC_000019.9:g.41523998C>A , CM000681.1:g.41523998C>A GRCh37
NC_000019.8:g.46215838C>A NCBI36
NG_007929.1:g.31795C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.*1266C>A MANE Select ENSP00000324648.2:n.*1266C>A
ENST00000324071.8:c.*1266C>A ENSP00000324648.2:n.*1266C>A
NM_000767.4:c.*1266C>A NP_000758.1:n.*1266C>A
XM_011526548.1:c.*1266C>A XP_011524850.1:n.*1266C>A
XM_011526549.1:c.*1266C>A XP_011524851.1:n.*1266C>A
XM_011526550.1:c.*1266C>A XP_011524852.1:n.*1266C>A
NM_000767.5:c.*1266C>A MANE Select NP_000758.1:n.*1266C>A
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