Canonical Allele Identifier: CA507537680

Gene: CYP2B6

Linked Data

• gnomAD v4: 19-41012431-T-C
• MyVariant Identifiers: chr19:g.41518336T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012431T>C , CM000681.2:g.41012431T>C	GRCh38
NC_000019.9:g.41518336T>C , CM000681.1:g.41518336T>C	GRCh37
NC_000019.8:g.46210176T>C	NCBI36
NG_007929.1:g.26133T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1098T>C MANE Select	ENSP00000324648.2:p.Gly366=
ENST00000598834.2:c.1122T>C
ENST00000324071.8:c.1098T>C	ENSP00000324648.2:p.Gly366=
ENST00000593831.1:c.390T>C	ENSP00000470582.1:p.Gly130=
ENST00000597612.1:n.593T>C
NM_000767.4:c.1098T>C	NP_000758.1:p.Gly366=
XM_005258569.3:c.1098T>C	XP_005258626.1:p.Gly366=
XM_006723050.2:c.1098T>C	XP_006723113.1:p.Gly366=
XM_011526546.1:c.1098T>C	XP_011524848.1:p.Gly366=
XM_011526547.1:c.1098T>C	XP_011524849.1:p.Gly366=
XM_011526548.1:c.618T>C	XP_011524850.1:p.Gly206=
XM_011526549.1:c.507T>C	XP_011524851.1:p.Gly169=
XM_011526550.1:c.498T>C	XP_011524852.1:p.Gly166=
NM_000767.5:c.1098T>C MANE Select	NP_000758.1:p.Gly366=