Canonical Allele Identifier: CA405984232

Gene: CYP2B6

Linked Data

• MyVariant Identifiers: chr19:g.41518233T>G (hg19) ; chr19:g.41012328T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012328T>G , CM000681.2:g.41012328T>G	GRCh38
NC_000019.9:g.41518233T>G , CM000681.1:g.41518233T>G	GRCh37
NC_000019.8:g.46210073T>G	NCBI36
NG_007929.1:g.26030T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000324071.10:c.995T>G MANE Select	ENSP00000324648.2:p.Ile332Ser
ENST00000598834.2:c.1019T>G
ENST00000324071.8:c.995T>G	ENSP00000324648.2:p.Ile332Ser
ENST00000593831.1:c.287T>G	ENSP00000470582.1:p.Ile96Ser
ENST00000597612.1:n.490T>G
NM_000767.4:c.995T>G	NP_000758.1:p.Ile332Ser
XM_005258569.3:c.995T>G	XP_005258626.1:p.Ile332Ser
XM_006723050.2:c.995T>G	XP_006723113.1:p.Ile332Ser
XM_011526546.1:c.995T>G	XP_011524848.1:p.Ile332Ser
XM_011526547.1:c.995T>G	XP_011524849.1:p.Ile332Ser
XM_011526548.1:c.515T>G	XP_011524850.1:p.Ile172Ser
XM_011526549.1:c.404T>G	XP_011524851.1:p.Ile135Ser
XM_011526550.1:c.395T>G	XP_011524852.1:p.Ile132Ser
NM_000767.5:c.995T>G MANE Select	NP_000758.1:p.Ile332Ser