Canonical Allele Identifier: CA507532734

Gene: CYP2B6

Linked Data

• gnomAD v4: 19-41004379-G-A
• MyVariant Identifiers: chr19:g.41510284G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41004379G>A , CM000681.2:g.41004379G>A	GRCh38
NC_000019.9:g.41510284G>A , CM000681.1:g.41510284G>A	GRCh37
NC_000019.8:g.46202124G>A	NCBI36
NG_007929.1:g.18081G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000324071.10:c.417G>A MANE Select	ENSP00000324648.2:p.Lys139=
ENST00000598834.2:c.319G>A
ENST00000324071.8:c.417G>A	ENSP00000324648.2:p.Lys139=
ENST00000593831.1:c.189G>A	ENSP00000470582.1:p.Lys63=
ENST00000594187.1:n.1G>A
ENST00000598834.1:n.319G>A
NM_000767.4:c.417G>A	NP_000758.1:p.Lys139=
XM_005258569.3:c.417G>A	XP_005258626.1:p.Lys139=
XM_006723050.2:c.417G>A	XP_006723113.1:p.Lys139=
XM_011526546.1:c.417G>A	XP_011524848.1:p.Lys139=
XM_011526547.1:c.417G>A	XP_011524849.1:p.Lys139=
XM_011526548.1:c.417G>A	XP_011524850.1:p.Lys139=
XM_011526549.1:c.-143G>A	XP_011524851.1:n.-143G>A
XM_011526550.1:c.297G>A	XP_011524852.1:p.Lys99=
NM_000767.5:c.417G>A MANE Select	NP_000758.1:p.Lys139=