Canonical Allele Identifier: CA405984397

Gene: CYP2B6

Linked Data

• MyVariant Identifiers: chr19:g.41518276G>A (hg19) ; chr19:g.41012371G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012371G>A , CM000681.2:g.41012371G>A	GRCh38
NC_000019.9:g.41518276G>A , CM000681.1:g.41518276G>A	GRCh37
NC_000019.8:g.46210116G>A	NCBI36
NG_007929.1:g.26073G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1038G>A MANE Select	ENSP00000324648.2:p.Met346Ile
ENST00000598834.2:c.1062G>A
ENST00000324071.8:c.1038G>A	ENSP00000324648.2:p.Met346Ile
ENST00000593831.1:c.330G>A	ENSP00000470582.1:p.Met110Ile
ENST00000597612.1:n.533G>A
NM_000767.4:c.1038G>A	NP_000758.1:p.Met346Ile
XM_005258569.3:c.1038G>A	XP_005258626.1:p.Met346Ile
XM_006723050.2:c.1038G>A	XP_006723113.1:p.Met346Ile
XM_011526546.1:c.1038G>A	XP_011524848.1:p.Met346Ile
XM_011526547.1:c.1038G>A	XP_011524849.1:p.Met346Ile
XM_011526548.1:c.558G>A	XP_011524850.1:p.Met186Ile
XM_011526549.1:c.447G>A	XP_011524851.1:p.Met149Ile
XM_011526550.1:c.438G>A	XP_011524852.1:p.Met146Ile
NM_000767.5:c.1038G>A MANE Select	NP_000758.1:p.Met346Ile