Canonical Allele Identifier: CA405984589

Gene: CYP2B6

Linked Data

• MyVariant Identifiers: chr19:g.41518320A>G (hg19) ; chr19:g.41012415A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012415A>G , CM000681.2:g.41012415A>G	GRCh38
NC_000019.9:g.41518320A>G , CM000681.1:g.41518320A>G	GRCh37
NC_000019.8:g.46210160A>G	NCBI36
NG_007929.1:g.26117A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1082A>G MANE Select	ENSP00000324648.2:p.Asp361Gly
ENST00000598834.2:c.1106A>G
ENST00000324071.8:c.1082A>G	ENSP00000324648.2:p.Asp361Gly
ENST00000593831.1:c.374A>G	ENSP00000470582.1:p.Asp125Gly
ENST00000597612.1:n.577A>G
NM_000767.4:c.1082A>G	NP_000758.1:p.Asp361Gly
XM_005258569.3:c.1082A>G	XP_005258626.1:p.Asp361Gly
XM_006723050.2:c.1082A>G	XP_006723113.1:p.Asp361Gly
XM_011526546.1:c.1082A>G	XP_011524848.1:p.Asp361Gly
XM_011526547.1:c.1082A>G	XP_011524849.1:p.Asp361Gly
XM_011526548.1:c.602A>G	XP_011524850.1:p.Asp201Gly
XM_011526549.1:c.491A>G	XP_011524851.1:p.Asp164Gly
XM_011526550.1:c.482A>G	XP_011524852.1:p.Asp161Gly
NM_000767.5:c.1082A>G MANE Select	NP_000758.1:p.Asp361Gly