Canonical Allele Identifier: CA405986155
Gene: CYP2B6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2303487
ClinVar RCV Id: RCV004148637

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41012737G>A , CM000681.2:g.41012737G>A GRCh38
NC_000019.9:g.41518642G>A , CM000681.1:g.41518642G>A GRCh37
NC_000019.8:g.46210482G>A NCBI36
NG_007929.1:g.26439G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.1216G>A MANE Select ENSP00000324648.2:p.Asp406Asn
ENST00000598834.2:c.1177-236G>A
ENST00000324071.8:c.1216G>A ENSP00000324648.2:p.Asp406Asn
ENST00000593831.1:c.508G>A ENSP00000470582.1:p.Asp170Asn
ENST00000597612.1:n.647+252G>A
NM_000767.4:c.1216G>A NP_000758.1:p.Asp406Asn
XM_005258569.3:c.1152+252G>A XP_005258626.1:n.1152+252G>A
XM_006723050.2:c.1216G>A XP_006723113.1:p.Asp406Asn
XM_011526546.1:c.1153-79G>A XP_011524848.1:n.1153-79G>A
XM_011526547.1:c.1153-236G>A XP_011524849.1:n.1153-236G>A
XM_011526548.1:c.736G>A XP_011524850.1:p.Asp246Asn
XM_011526549.1:c.625G>A XP_011524851.1:p.Asp209Asn
XM_011526550.1:c.616G>A XP_011524852.1:p.Asp206Asn
NM_000767.5:c.1216G>A MANE Select NP_000758.1:p.Asp406Asn