Canonical Allele Identifier: CA507537632

Gene: CYP2B6

Linked Data

• MyVariant Identifiers: chr19:g.41518294C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012389C>G , CM000681.2:g.41012389C>G	GRCh38
NC_000019.9:g.41518294C>G , CM000681.1:g.41518294C>G	GRCh37
NC_000019.8:g.46210134C>G	NCBI36
NG_007929.1:g.26091C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1056C>G MANE Select	ENSP00000324648.2:p.Val352=
ENST00000598834.2:c.1080C>G
ENST00000324071.8:c.1056C>G	ENSP00000324648.2:p.Val352=
ENST00000593831.1:c.348C>G	ENSP00000470582.1:p.Val116=
ENST00000597612.1:n.551C>G
NM_000767.4:c.1056C>G	NP_000758.1:p.Val352=
XM_005258569.3:c.1056C>G	XP_005258626.1:p.Val352=
XM_006723050.2:c.1056C>G	XP_006723113.1:p.Val352=
XM_011526546.1:c.1056C>G	XP_011524848.1:p.Val352=
XM_011526547.1:c.1056C>G	XP_011524849.1:p.Val352=
XM_011526548.1:c.576C>G	XP_011524850.1:p.Val192=
XM_011526549.1:c.465C>G	XP_011524851.1:p.Val155=
XM_011526550.1:c.456C>G	XP_011524852.1:p.Val152=
NM_000767.5:c.1056C>G MANE Select	NP_000758.1:p.Val352=