Canonical Allele Identifier: CA308470403

Gene: CYP2B6

Linked Data

• dbSNP Id: rs3211371
• gnomAD v4: 19-41016810-C-G
• MyVariant Identifiers: chr19:g.41522715C>G (hg19) ; chr19:g.41016810C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41016810C>G , CM000681.2:g.41016810C>G	GRCh38
NC_000019.9:g.41522715C>G , CM000681.1:g.41522715C>G	GRCh37
NC_000019.8:g.46214555C>G	NCBI36
NG_007929.1:g.30512C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000324071.10:c.1459C>G MANE Select	ENSP00000324648.2:p.Arg487Gly
ENST00000598834.2:c.1399C>G
ENST00000324071.8:c.1459C>G	ENSP00000324648.2:p.Arg487Gly
ENST00000593831.1:c.751C>G	ENSP00000470582.1:p.Arg251Gly
ENST00000597612.1:n.812C>G
NM_000767.4:c.1459C>G	NP_000758.1:p.Arg487Gly
XM_005258569.3:c.*48C>G	XP_005258626.1:n.*48C>G
XM_011526548.1:c.979C>G	XP_011524850.1:p.Arg327Gly
XM_011526549.1:c.868C>G	XP_011524851.1:p.Arg290Gly
XM_011526550.1:c.859C>G	XP_011524852.1:p.Arg287Gly
NM_000767.5:c.1459C>G MANE Select	NP_000758.1:p.Arg487Gly