Canonical Allele Identifier: CA507535633

Gene: CYP2B6

Linked Data

• MyVariant Identifiers: chr19:g.41515285G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41009380G>C , CM000681.2:g.41009380G>C	GRCh38
NC_000019.9:g.41515285G>C , CM000681.1:g.41515285G>C	GRCh37
NC_000019.8:g.46207125G>C	NCBI36
NG_007929.1:g.23082G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.807G>C MANE Select	ENSP00000324648.2:p.Leu269=
ENST00000598834.2:c.831G>C
ENST00000324071.8:c.807G>C	ENSP00000324648.2:p.Leu269=
ENST00000593831.1:c.257-2918G>C	ENSP00000470582.1:n.257-2918G>C
NM_000767.4:c.807G>C	NP_000758.1:p.Leu269=
XM_005258569.3:c.807G>C	XP_005258626.1:p.Leu269=
XM_006723050.2:c.807G>C	XP_006723113.1:p.Leu269=
XM_011526546.1:c.807G>C	XP_011524848.1:p.Leu269=
XM_011526547.1:c.807G>C	XP_011524849.1:p.Leu269=
XM_011526548.1:c.485-2918G>C	XP_011524850.1:n.485-2918G>C
XM_011526549.1:c.216G>C	XP_011524851.1:p.Leu72=
XM_011526550.1:c.365-2918G>C	XP_011524852.1:n.365-2918G>C
NM_000767.5:c.807G>C MANE Select	NP_000758.1:p.Leu269=