Canonical Allele Identifier: CA507537547

Gene: CYP2B6

Linked Data

• gnomAD v4: 19-41012317-T-C
• MyVariant Identifiers: chr19:g.41518222T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012317T>C , CM000681.2:g.41012317T>C	GRCh38
NC_000019.9:g.41518222T>C , CM000681.1:g.41518222T>C	GRCh37
NC_000019.8:g.46210062T>C	NCBI36
NG_007929.1:g.26019T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000324071.10:c.984T>C MANE Select	ENSP00000324648.2:p.Ile328=
ENST00000598834.2:c.1008T>C
ENST00000324071.8:c.984T>C	ENSP00000324648.2:p.Ile328=
ENST00000593831.1:c.276T>C	ENSP00000470582.1:p.Ile92=
ENST00000597612.1:n.479T>C
NM_000767.4:c.984T>C	NP_000758.1:p.Ile328=
XM_005258569.3:c.984T>C	XP_005258626.1:p.Ile328=
XM_006723050.2:c.984T>C	XP_006723113.1:p.Ile328=
XM_011526546.1:c.984T>C	XP_011524848.1:p.Ile328=
XM_011526547.1:c.984T>C	XP_011524849.1:p.Ile328=
XM_011526548.1:c.504T>C	XP_011524850.1:p.Ile168=
XM_011526549.1:c.393T>C	XP_011524851.1:p.Ile131=
XM_011526550.1:c.384T>C	XP_011524852.1:p.Ile128=
NM_000767.5:c.984T>C MANE Select	NP_000758.1:p.Ile328=