Canonical Allele Identifier: CA405980765

Gene: CYP2B6

Linked Data

• MyVariant Identifiers: chr19:g.41515269T>G (hg19) ; chr19:g.41009364T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41009364T>G , CM000681.2:g.41009364T>G	GRCh38
NC_000019.9:g.41515269T>G , CM000681.1:g.41515269T>G	GRCh37
NC_000019.8:g.46207109T>G	NCBI36
NG_007929.1:g.23066T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000324071.10:c.791T>G MANE Select	ENSP00000324648.2:p.Leu264Arg
ENST00000598834.2:c.815T>G
ENST00000324071.8:c.791T>G	ENSP00000324648.2:p.Leu264Arg
ENST00000593831.1:c.257-2934T>G	ENSP00000470582.1:n.257-2934T>G
NM_000767.4:c.791T>G	NP_000758.1:p.Leu264Arg
XM_005258569.3:c.791T>G	XP_005258626.1:p.Leu264Arg
XM_006723050.2:c.791T>G	XP_006723113.1:p.Leu264Arg
XM_011526546.1:c.791T>G	XP_011524848.1:p.Leu264Arg
XM_011526547.1:c.791T>G	XP_011524849.1:p.Leu264Arg
XM_011526548.1:c.485-2934T>G	XP_011524850.1:n.485-2934T>G
XM_011526549.1:c.200T>G	XP_011524851.1:p.Leu67Arg
XM_011526550.1:c.365-2934T>G	XP_011524852.1:n.365-2934T>G
NM_000767.5:c.791T>G MANE Select	NP_000758.1:p.Leu264Arg