Canonical Allele Identifier: CA405984680
Gene: CYP2B6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41012438C>G , CM000681.2:g.41012438C>G GRCh38
NC_000019.9:g.41518343C>G , CM000681.1:g.41518343C>G GRCh37
NC_000019.8:g.46210183C>G NCBI36
NG_007929.1:g.26140C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.1105C>G MANE Select ENSP00000324648.2:p.His369Asp
ENST00000598834.2:c.1129C>G
ENST00000324071.8:c.1105C>G ENSP00000324648.2:p.His369Asp
ENST00000593831.1:c.397C>G ENSP00000470582.1:p.His133Asp
ENST00000597612.1:n.600C>G
NM_000767.4:c.1105C>G NP_000758.1:p.His369Asp
XM_005258569.3:c.1105C>G XP_005258626.1:p.His369Asp
XM_006723050.2:c.1105C>G XP_006723113.1:p.His369Asp
XM_011526546.1:c.1105C>G XP_011524848.1:p.His369Asp
XM_011526547.1:c.1105C>G XP_011524849.1:p.His369Asp
XM_011526548.1:c.625C>G XP_011524850.1:p.His209Asp
XM_011526549.1:c.514C>G XP_011524851.1:p.His172Asp
XM_011526550.1:c.505C>G XP_011524852.1:p.His169Asp
NM_000767.5:c.1105C>G MANE Select NP_000758.1:p.His369Asp