Canonical Allele Identifier: CA308499187

Gene: CYP2B6

Linked Data

• dbSNP Id: rs990408094
• MyVariant Identifiers: chr19:g.41518224A>T (hg19) ; chr19:g.41012319A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012319A>T , CM000681.2:g.41012319A>T	GRCh38
NC_000019.9:g.41518224A>T , CM000681.1:g.41518224A>T	GRCh37
NC_000019.8:g.46210064A>T	NCBI36
NG_007929.1:g.26021A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324071.10:c.986A>T MANE Select	ENSP00000324648.2:p.Glu329Val
ENST00000598834.2:c.1010A>T
ENST00000324071.8:c.986A>T	ENSP00000324648.2:p.Glu329Val
ENST00000593831.1:c.278A>T	ENSP00000470582.1:p.Glu93Val
ENST00000597612.1:n.481A>T
NM_000767.4:c.986A>T	NP_000758.1:p.Glu329Val
XM_005258569.3:c.986A>T	XP_005258626.1:p.Glu329Val
XM_006723050.2:c.986A>T	XP_006723113.1:p.Glu329Val
XM_011526546.1:c.986A>T	XP_011524848.1:p.Glu329Val
XM_011526547.1:c.986A>T	XP_011524849.1:p.Glu329Val
XM_011526548.1:c.506A>T	XP_011524850.1:p.Glu169Val
XM_011526549.1:c.395A>T	XP_011524851.1:p.Glu132Val
XM_011526550.1:c.386A>T	XP_011524852.1:p.Glu129Val
NM_000767.5:c.986A>T MANE Select	NP_000758.1:p.Glu329Val