Canonical Allele Identifier: CA405980791

Gene: CYP2B6

Linked Data

• MyVariant Identifiers: chr19:g.41515277A>C (hg19) ; chr19:g.41009372A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41009372A>C , CM000681.2:g.41009372A>C	GRCh38
NC_000019.9:g.41515277A>C , CM000681.1:g.41515277A>C	GRCh37
NC_000019.8:g.46207117A>C	NCBI36
NG_007929.1:g.23074A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000324071.10:c.799A>C MANE Select	ENSP00000324648.2:p.Thr267Pro
ENST00000598834.2:c.823A>C
ENST00000324071.8:c.799A>C	ENSP00000324648.2:p.Thr267Pro
ENST00000593831.1:c.257-2926A>C	ENSP00000470582.1:n.257-2926A>C
NM_000767.4:c.799A>C	NP_000758.1:p.Thr267Pro
XM_005258569.3:c.799A>C	XP_005258626.1:p.Thr267Pro
XM_006723050.2:c.799A>C	XP_006723113.1:p.Thr267Pro
XM_011526546.1:c.799A>C	XP_011524848.1:p.Thr267Pro
XM_011526547.1:c.799A>C	XP_011524849.1:p.Thr267Pro
XM_011526548.1:c.485-2926A>C	XP_011524850.1:n.485-2926A>C
XM_011526549.1:c.208A>C	XP_011524851.1:p.Thr70Pro
XM_011526550.1:c.365-2926A>C	XP_011524852.1:n.365-2926A>C
NM_000767.5:c.799A>C MANE Select	NP_000758.1:p.Thr267Pro