Canonical Allele Identifier: CA405974987

Gene: CYP2B6

Linked Data

• MyVariant Identifiers: chr19:g.41510284G>C (hg19) ; chr19:g.41004379G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41004379G>C , CM000681.2:g.41004379G>C	GRCh38
NC_000019.9:g.41510284G>C , CM000681.1:g.41510284G>C	GRCh37
NC_000019.8:g.46202124G>C	NCBI36
NG_007929.1:g.18081G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000324071.10:c.417G>C MANE Select	ENSP00000324648.2:p.Lys139Asn
ENST00000598834.2:c.319G>C
ENST00000324071.8:c.417G>C	ENSP00000324648.2:p.Lys139Asn
ENST00000593831.1:c.189G>C	ENSP00000470582.1:p.Lys63Asn
ENST00000594187.1:n.1G>C
ENST00000598834.1:n.319G>C
NM_000767.4:c.417G>C	NP_000758.1:p.Lys139Asn
XM_005258569.3:c.417G>C	XP_005258626.1:p.Lys139Asn
XM_006723050.2:c.417G>C	XP_006723113.1:p.Lys139Asn
XM_011526546.1:c.417G>C	XP_011524848.1:p.Lys139Asn
XM_011526547.1:c.417G>C	XP_011524849.1:p.Lys139Asn
XM_011526548.1:c.417G>C	XP_011524850.1:p.Lys139Asn
XM_011526549.1:c.-143G>C	XP_011524851.1:n.-143G>C
XM_011526550.1:c.297G>C	XP_011524852.1:p.Lys99Asn
NM_000767.5:c.417G>C MANE Select	NP_000758.1:p.Lys139Asn