Canonical Allele Identifier: CA882289456

Gene: CYP2B6

Linked Data

• dbSNP Id: rs1201507124
• gnomAD v3: 19-41012872-C-A
• gnomAD v4: 19-41012872-C-A
• MyVariant Identifiers: chr19:g.41518777C>A (hg19) ; chr19:g.41012872C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012872C>A , CM000681.2:g.41012872C>A	GRCh38
NC_000019.9:g.41518777C>A , CM000681.1:g.41518777C>A	GRCh37
NC_000019.8:g.46210617C>A	NCBI36
NG_007929.1:g.26574C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1294+57C>A MANE Select	ENSP00000324648.2:n.1294+57C>A
ENST00000598834.2:c.1177-101C>A
ENST00000324071.8:c.1294+57C>A	ENSP00000324648.2:n.1294+57C>A
ENST00000593831.1:c.586+57C>A	ENSP00000470582.1:n.586+57C>A
ENST00000597612.1:n.647+387C>A
NM_000767.4:c.1294+57C>A	NP_000758.1:n.1294+57C>A
XM_005258569.3:c.1152+387C>A	XP_005258626.1:n.1152+387C>A
XM_006723050.2:c.1294+57C>A	XP_006723113.1:n.1294+57C>A
XM_011526546.1:c.1209C>A	XP_011524848.1:p.Asn403Lys
XM_011526547.1:c.1153-101C>A	XP_011524849.1:n.1153-101C>A
XM_011526548.1:c.814+57C>A	XP_011524850.1:n.814+57C>A
XM_011526549.1:c.703+57C>A	XP_011524851.1:n.703+57C>A
XM_011526550.1:c.694+57C>A	XP_011524852.1:n.694+57C>A
NM_000767.5:c.1294+57C>A MANE Select	NP_000758.1:n.1294+57C>A