Canonical Allele Identifier: CA2576790775

Gene: CYP2B6

Linked Data

• gnomAD v4: 19-41012861-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012861A>C , CM000681.2:g.41012861A>C	GRCh38
NC_000019.9:g.41518766A>C , CM000681.1:g.41518766A>C	GRCh37
NC_000019.8:g.46210606A>C	NCBI36
NG_007929.1:g.26563A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1294+46A>C MANE Select	ENSP00000324648.2:n.1294+46A>C
ENST00000598834.2:c.1177-112A>C
ENST00000324071.8:c.1294+46A>C	ENSP00000324648.2:n.1294+46A>C
ENST00000593831.1:c.586+46A>C	ENSP00000470582.1:n.586+46A>C
ENST00000597612.1:n.647+376A>C
NM_000767.4:c.1294+46A>C	NP_000758.1:n.1294+46A>C
XM_005258569.3:c.1152+376A>C	XP_005258626.1:n.1152+376A>C
XM_006723050.2:c.1294+46A>C	XP_006723113.1:n.1294+46A>C
XM_011526546.1:c.1198A>C	XP_011524848.1:p.Thr400Pro
XM_011526547.1:c.1153-112A>C	XP_011524849.1:n.1153-112A>C
XM_011526548.1:c.814+46A>C	XP_011524850.1:n.814+46A>C
XM_011526549.1:c.703+46A>C	XP_011524851.1:n.703+46A>C
XM_011526550.1:c.694+46A>C	XP_011524852.1:n.694+46A>C
NM_000767.5:c.1294+46A>C MANE Select	NP_000758.1:n.1294+46A>C