Canonical Allele Identifier: CA507535605

Gene: CYP2B6

Linked Data

• dbSNP Id: rs189970623
• gnomAD v3: 19-41009368-C-A
• gnomAD v4: 19-41009368-C-A
• MyVariant Identifiers: chr19:g.41515273C>A (hg19) ; chr19:g.41009368C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41009368C>A , CM000681.2:g.41009368C>A	GRCh38
NC_000019.9:g.41515273C>A , CM000681.1:g.41515273C>A	GRCh37
NC_000019.8:g.46207113C>A	NCBI36
NG_007929.1:g.23070C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000324071.10:c.795C>A MANE Select	ENSP00000324648.2:p.Ile265=
ENST00000598834.2:c.819C>A
ENST00000324071.8:c.795C>A	ENSP00000324648.2:p.Ile265=
ENST00000593831.1:c.257-2930C>A	ENSP00000470582.1:n.257-2930C>A
NM_000767.4:c.795C>A	NP_000758.1:p.Ile265=
XM_005258569.3:c.795C>A	XP_005258626.1:p.Ile265=
XM_006723050.2:c.795C>A	XP_006723113.1:p.Ile265=
XM_011526546.1:c.795C>A	XP_011524848.1:p.Ile265=
XM_011526547.1:c.795C>A	XP_011524849.1:p.Ile265=
XM_011526548.1:c.485-2930C>A	XP_011524850.1:n.485-2930C>A
XM_011526549.1:c.204C>A	XP_011524851.1:p.Ile68=
XM_011526550.1:c.365-2930C>A	XP_011524852.1:n.365-2930C>A
NM_000767.5:c.795C>A MANE Select	NP_000758.1:p.Ile265=