Canonical Allele Identifier: CA2576790776

Gene: CYP2B6

Linked Data

• gnomAD v4: 19-41012865-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012865T>C , CM000681.2:g.41012865T>C	GRCh38
NC_000019.9:g.41518770T>C , CM000681.1:g.41518770T>C	GRCh37
NC_000019.8:g.46210610T>C	NCBI36
NG_007929.1:g.26567T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1294+50T>C MANE Select	ENSP00000324648.2:n.1294+50T>C
ENST00000598834.2:c.1177-108T>C
ENST00000324071.8:c.1294+50T>C	ENSP00000324648.2:n.1294+50T>C
ENST00000593831.1:c.586+50T>C	ENSP00000470582.1:n.586+50T>C
ENST00000597612.1:n.647+380T>C
NM_000767.4:c.1294+50T>C	NP_000758.1:n.1294+50T>C
XM_005258569.3:c.1152+380T>C	XP_005258626.1:n.1152+380T>C
XM_006723050.2:c.1294+50T>C	XP_006723113.1:n.1294+50T>C
XM_011526546.1:c.1202T>C	XP_011524848.1:p.Ile401Thr
XM_011526547.1:c.1153-108T>C	XP_011524849.1:n.1153-108T>C
XM_011526548.1:c.814+50T>C	XP_011524850.1:n.814+50T>C
XM_011526549.1:c.703+50T>C	XP_011524851.1:n.703+50T>C
XM_011526550.1:c.694+50T>C	XP_011524852.1:n.694+50T>C
NM_000767.5:c.1294+50T>C MANE Select	NP_000758.1:n.1294+50T>C