Canonical Allele Identifier: CA507537558

Gene: CYP2B6

Linked Data

• MyVariant Identifiers: chr19:g.41518231G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012326G>T , CM000681.2:g.41012326G>T	GRCh38
NC_000019.9:g.41518231G>T , CM000681.1:g.41518231G>T	GRCh37
NC_000019.8:g.46210071G>T	NCBI36
NG_007929.1:g.26028G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324071.10:c.993G>T MANE Select	ENSP00000324648.2:p.Val331=
ENST00000598834.2:c.1017G>T
ENST00000324071.8:c.993G>T	ENSP00000324648.2:p.Val331=
ENST00000593831.1:c.285G>T	ENSP00000470582.1:p.Val95=
ENST00000597612.1:n.488G>T
NM_000767.4:c.993G>T	NP_000758.1:p.Val331=
XM_005258569.3:c.993G>T	XP_005258626.1:p.Val331=
XM_006723050.2:c.993G>T	XP_006723113.1:p.Val331=
XM_011526546.1:c.993G>T	XP_011524848.1:p.Val331=
XM_011526547.1:c.993G>T	XP_011524849.1:p.Val331=
XM_011526548.1:c.513G>T	XP_011524850.1:p.Val171=
XM_011526549.1:c.402G>T	XP_011524851.1:p.Val134=
XM_011526550.1:c.393G>T	XP_011524852.1:p.Val131=
NM_000767.5:c.993G>T MANE Select	NP_000758.1:p.Val331=