Canonical Allele Identifier: CA405985971

Gene: CYP2B6

Linked Data

• COSMIC: COSM996890
• MyVariant Identifiers: chr19:g.41518600C>A (hg19) ; chr19:g.41012695C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012695C>A , CM000681.2:g.41012695C>A	GRCh38
NC_000019.9:g.41518600C>A , CM000681.1:g.41518600C>A	GRCh37
NC_000019.8:g.46210440C>A	NCBI36
NG_007929.1:g.26397C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1174C>A MANE Select	ENSP00000324648.2:p.Leu392Met
ENST00000598834.2:c.1176+210C>A
ENST00000324071.8:c.1174C>A	ENSP00000324648.2:p.Leu392Met
ENST00000593831.1:c.466C>A	ENSP00000470582.1:p.Leu156Met
ENST00000597612.1:n.647+210C>A
NM_000767.4:c.1174C>A	NP_000758.1:p.Leu392Met
XM_005258569.3:c.1152+210C>A	XP_005258626.1:n.1152+210C>A
XM_006723050.2:c.1174C>A	XP_006723113.1:p.Leu392Met
XM_011526546.1:c.1153-121C>A	XP_011524848.1:n.1153-121C>A
XM_011526547.1:c.1152+210C>A	XP_011524849.1:n.1152+210C>A
XM_011526548.1:c.694C>A	XP_011524850.1:p.Leu232Met
XM_011526549.1:c.583C>A	XP_011524851.1:p.Leu195Met
XM_011526550.1:c.574C>A	XP_011524852.1:p.Leu192Met
NM_000767.5:c.1174C>A MANE Select	NP_000758.1:p.Leu392Met