Canonical Allele Identifier: CA405984220

Gene: CYP2B6

Linked Data

• MyVariant Identifiers: chr19:g.41518229G>A (hg19) ; chr19:g.41012324G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012324G>A , CM000681.2:g.41012324G>A	GRCh38
NC_000019.9:g.41518229G>A , CM000681.1:g.41518229G>A	GRCh37
NC_000019.8:g.46210069G>A	NCBI36
NG_007929.1:g.26026G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000324071.10:c.991G>A MANE Select	ENSP00000324648.2:p.Val331Met
ENST00000598834.2:c.1015G>A
ENST00000324071.8:c.991G>A	ENSP00000324648.2:p.Val331Met
ENST00000593831.1:c.283G>A	ENSP00000470582.1:p.Val95Met
ENST00000597612.1:n.486G>A
NM_000767.4:c.991G>A	NP_000758.1:p.Val331Met
XM_005258569.3:c.991G>A	XP_005258626.1:p.Val331Met
XM_006723050.2:c.991G>A	XP_006723113.1:p.Val331Met
XM_011526546.1:c.991G>A	XP_011524848.1:p.Val331Met
XM_011526547.1:c.991G>A	XP_011524849.1:p.Val331Met
XM_011526548.1:c.511G>A	XP_011524850.1:p.Val171Met
XM_011526549.1:c.400G>A	XP_011524851.1:p.Val134Met
XM_011526550.1:c.391G>A	XP_011524852.1:p.Val131Met
NM_000767.5:c.991G>A MANE Select	NP_000758.1:p.Val331Met