Canonical Allele Identifier: CA507538296

Gene: CYP2B6

Linked Data

• MyVariant Identifiers: chr19:g.41518635A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012730A>G , CM000681.2:g.41012730A>G	GRCh38
NC_000019.9:g.41518635A>G , CM000681.1:g.41518635A>G	GRCh37
NC_000019.8:g.46210475A>G	NCBI36
NG_007929.1:g.26432A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1209A>G MANE Select	ENSP00000324648.2:p.Glu403=
ENST00000598834.2:c.1177-243A>G
ENST00000324071.8:c.1209A>G	ENSP00000324648.2:p.Glu403=
ENST00000593831.1:c.501A>G	ENSP00000470582.1:p.Glu167=
ENST00000597612.1:n.647+245A>G
NM_000767.4:c.1209A>G	NP_000758.1:p.Glu403=
XM_005258569.3:c.1152+245A>G	XP_005258626.1:n.1152+245A>G
XM_006723050.2:c.1209A>G	XP_006723113.1:p.Glu403=
XM_011526546.1:c.1153-86A>G	XP_011524848.1:n.1153-86A>G
XM_011526547.1:c.1153-243A>G	XP_011524849.1:n.1153-243A>G
XM_011526548.1:c.729A>G	XP_011524850.1:p.Glu243=
XM_011526549.1:c.618A>G	XP_011524851.1:p.Glu206=
XM_011526550.1:c.609A>G	XP_011524852.1:p.Glu203=
NM_000767.5:c.1209A>G MANE Select	NP_000758.1:p.Glu403=