Canonical Allele Identifier: CA405986027

Gene: CYP2B6

Linked Data

• dbSNP Id: rs1568563433
• gnomAD v4: 19-41012707-C-G
• MyVariant Identifiers: chr19:g.41518612C>G (hg19) ; chr19:g.41012707C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012707C>G , CM000681.2:g.41012707C>G	GRCh38
NC_000019.9:g.41518612C>G , CM000681.1:g.41518612C>G	GRCh37
NC_000019.8:g.46210452C>G	NCBI36
NG_007929.1:g.26409C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1186C>G MANE Select	ENSP00000324648.2:p.Leu396Val
ENST00000598834.2:c.1176+222C>G
ENST00000324071.8:c.1186C>G	ENSP00000324648.2:p.Leu396Val
ENST00000593831.1:c.478C>G	ENSP00000470582.1:p.Leu160Val
ENST00000597612.1:n.647+222C>G
NM_000767.4:c.1186C>G	NP_000758.1:p.Leu396Val
XM_005258569.3:c.1152+222C>G	XP_005258626.1:n.1152+222C>G
XM_006723050.2:c.1186C>G	XP_006723113.1:p.Leu396Val
XM_011526546.1:c.1153-109C>G	XP_011524848.1:n.1153-109C>G
XM_011526547.1:c.1152+222C>G	XP_011524849.1:n.1152+222C>G
XM_011526548.1:c.706C>G	XP_011524850.1:p.Leu236Val
XM_011526549.1:c.595C>G	XP_011524851.1:p.Leu199Val
XM_011526550.1:c.586C>G	XP_011524852.1:p.Leu196Val
NM_000767.5:c.1186C>G MANE Select	NP_000758.1:p.Leu396Val