Canonical Allele Identifier: CA405984860

Gene: CYP2B6

Linked Data

• COSMIC: COSM5698335
• MyVariant Identifiers: chr19:g.41518385C>A (hg19) ; chr19:g.41012480C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012480C>A , CM000681.2:g.41012480C>A	GRCh38
NC_000019.9:g.41518385C>A , CM000681.1:g.41518385C>A	GRCh37
NC_000019.8:g.46210225C>A	NCBI36
NG_007929.1:g.26182C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1147C>A MANE Select	ENSP00000324648.2:p.Pro383Thr
ENST00000598834.2:c.1171C>A
ENST00000324071.8:c.1147C>A	ENSP00000324648.2:p.Pro383Thr
ENST00000593831.1:c.439C>A	ENSP00000470582.1:p.Pro147Thr
ENST00000597612.1:n.642C>A
NM_000767.4:c.1147C>A	NP_000758.1:p.Pro383Thr
XM_005258569.3:c.1147C>A	XP_005258626.1:p.Pro383Thr
XM_006723050.2:c.1147C>A	XP_006723113.1:p.Pro383Thr
XM_011526546.1:c.1147C>A	XP_011524848.1:p.Pro383Thr
XM_011526547.1:c.1147C>A	XP_011524849.1:p.Pro383Thr
XM_011526548.1:c.667C>A	XP_011524850.1:p.Pro223Thr
XM_011526549.1:c.556C>A	XP_011524851.1:p.Pro186Thr
XM_011526550.1:c.547C>A	XP_011524852.1:p.Pro183Thr
NM_000767.5:c.1147C>A MANE Select	NP_000758.1:p.Pro383Thr