Canonical Allele Identifier: CA405977585

Gene: CYP2B6

Linked Data

• MyVariant Identifiers: chr19:g.41512883A>T (hg19) ; chr19:g.41006978A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41006978A>T , CM000681.2:g.41006978A>T	GRCh38
NC_000019.9:g.41512883A>T , CM000681.1:g.41512883A>T	GRCh37
NC_000019.8:g.46204723A>T	NCBI36
NG_007929.1:g.20680A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.558A>T MANE Select	ENSP00000324648.2:p.Lys186Asn
ENST00000598834.2:c.460A>T
ENST00000324071.8:c.558A>T	ENSP00000324648.2:p.Lys186Asn
ENST00000593831.1:c.256+2532A>T	ENSP00000470582.1:n.256+2532A>T
ENST00000594187.1:n.142A>T
ENST00000598834.1:n.460A>T
NM_000767.4:c.558A>T	NP_000758.1:p.Lys186Asn
XM_005258569.3:c.558A>T	XP_005258626.1:p.Lys186Asn
XM_006723050.2:c.558A>T	XP_006723113.1:p.Lys186Asn
XM_011526546.1:c.558A>T	XP_011524848.1:p.Lys186Asn
XM_011526547.1:c.558A>T	XP_011524849.1:p.Lys186Asn
XM_011526548.1:c.484+2532A>T	XP_011524850.1:n.484+2532A>T
XM_011526549.1:c.-34A>T	XP_011524851.1:n.-34A>T
XM_011526550.1:c.364+2532A>T	XP_011524852.1:n.364+2532A>T
NM_000767.5:c.558A>T MANE Select	NP_000758.1:p.Lys186Asn