Canonical Allele Identifier: CA405984524

Gene: CYP2B6

Linked Data

• MyVariant Identifiers: chr19:g.41518305T>C (hg19) ; chr19:g.41012400T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012400T>C , CM000681.2:g.41012400T>C	GRCh38
NC_000019.9:g.41518305T>C , CM000681.1:g.41518305T>C	GRCh37
NC_000019.8:g.46210145T>C	NCBI36
NG_007929.1:g.26102T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1067T>C MANE Select	ENSP00000324648.2:p.Ile356Thr
ENST00000598834.2:c.1091T>C
ENST00000324071.8:c.1067T>C	ENSP00000324648.2:p.Ile356Thr
ENST00000593831.1:c.359T>C	ENSP00000470582.1:p.Ile120Thr
ENST00000597612.1:n.562T>C
NM_000767.4:c.1067T>C	NP_000758.1:p.Ile356Thr
XM_005258569.3:c.1067T>C	XP_005258626.1:p.Ile356Thr
XM_006723050.2:c.1067T>C	XP_006723113.1:p.Ile356Thr
XM_011526546.1:c.1067T>C	XP_011524848.1:p.Ile356Thr
XM_011526547.1:c.1067T>C	XP_011524849.1:p.Ile356Thr
XM_011526548.1:c.587T>C	XP_011524850.1:p.Ile196Thr
XM_011526549.1:c.476T>C	XP_011524851.1:p.Ile159Thr
XM_011526550.1:c.467T>C	XP_011524852.1:p.Ile156Thr
NM_000767.5:c.1067T>C MANE Select	NP_000758.1:p.Ile356Thr