Canonical Allele Identifier: CA507538323

Gene: CYP2B6

Linked Data

• MyVariant Identifiers: chr19:g.41518641A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012736A>T , CM000681.2:g.41012736A>T	GRCh38
NC_000019.9:g.41518641A>T , CM000681.1:g.41518641A>T	GRCh37
NC_000019.8:g.46210481A>T	NCBI36
NG_007929.1:g.26438A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1215A>T MANE Select	ENSP00000324648.2:p.Pro405=
ENST00000598834.2:c.1177-237A>T
ENST00000324071.8:c.1215A>T	ENSP00000324648.2:p.Pro405=
ENST00000593831.1:c.507A>T	ENSP00000470582.1:p.Pro169=
ENST00000597612.1:n.647+251A>T
NM_000767.4:c.1215A>T	NP_000758.1:p.Pro405=
XM_005258569.3:c.1152+251A>T	XP_005258626.1:n.1152+251A>T
XM_006723050.2:c.1215A>T	XP_006723113.1:p.Pro405=
XM_011526546.1:c.1153-80A>T	XP_011524848.1:n.1153-80A>T
XM_011526547.1:c.1153-237A>T	XP_011524849.1:n.1153-237A>T
XM_011526548.1:c.735A>T	XP_011524850.1:p.Pro245=
XM_011526549.1:c.624A>T	XP_011524851.1:p.Pro208=
XM_011526550.1:c.615A>T	XP_011524852.1:p.Pro205=
NM_000767.5:c.1215A>T MANE Select	NP_000758.1:p.Pro405=