Canonical Allele Identifier: CA507538432

Gene: CYP2B6

Linked Data

• MyVariant Identifiers: chr19:g.41518668G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012763G>C , CM000681.2:g.41012763G>C	GRCh38
NC_000019.9:g.41518668G>C , CM000681.1:g.41518668G>C	GRCh37
NC_000019.8:g.46210508G>C	NCBI36
NG_007929.1:g.26465G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1242G>C MANE Select	ENSP00000324648.2:p.Leu414=
ENST00000598834.2:c.1177-210G>C
ENST00000324071.8:c.1242G>C	ENSP00000324648.2:p.Leu414=
ENST00000593831.1:c.534G>C	ENSP00000470582.1:p.Leu178=
ENST00000597612.1:n.647+278G>C
NM_000767.4:c.1242G>C	NP_000758.1:p.Leu414=
XM_005258569.3:c.1152+278G>C	XP_005258626.1:n.1152+278G>C
XM_006723050.2:c.1242G>C	XP_006723113.1:p.Leu414=
XM_011526546.1:c.1153-53G>C	XP_011524848.1:n.1153-53G>C
XM_011526547.1:c.1153-210G>C	XP_011524849.1:n.1153-210G>C
XM_011526548.1:c.762G>C	XP_011524850.1:p.Leu254=
XM_011526549.1:c.651G>C	XP_011524851.1:p.Leu217=
XM_011526550.1:c.642G>C	XP_011524852.1:p.Leu214=
NM_000767.5:c.1242G>C MANE Select	NP_000758.1:p.Leu414=