Canonical Allele Identifier: CA2585217038

Gene: CYP2B6

Linked Data

• gnomAD v4: 19-41012216-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012216C>A , CM000681.2:g.41012216C>A	GRCh38
NC_000019.9:g.41518121C>A , CM000681.1:g.41518121C>A	GRCh37
NC_000019.8:g.46209961C>A	NCBI36
NG_007929.1:g.25918C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000324071.10:c.965-82C>A MANE Select	ENSP00000324648.2:n.965-82C>A
ENST00000598834.2:c.989-82C>A
ENST00000324071.8:c.965-82C>A	ENSP00000324648.2:n.965-82C>A
ENST00000593831.1:c.257-82C>A	ENSP00000470582.1:n.257-82C>A
ENST00000597612.1:n.460-82C>A
NM_000767.4:c.965-82C>A	NP_000758.1:n.965-82C>A
XM_005258569.3:c.965-82C>A	XP_005258626.1:n.965-82C>A
XM_006723050.2:c.965-82C>A	XP_006723113.1:n.965-82C>A
XM_011526546.1:c.965-82C>A	XP_011524848.1:n.965-82C>A
XM_011526547.1:c.965-82C>A	XP_011524849.1:n.965-82C>A
XM_011526548.1:c.485-82C>A	XP_011524850.1:n.485-82C>A
XM_011526549.1:c.374-82C>A	XP_011524851.1:n.374-82C>A
XM_011526550.1:c.365-82C>A	XP_011524852.1:n.365-82C>A
NM_000767.5:c.965-82C>A MANE Select	NP_000758.1:n.965-82C>A