Canonical Allele Identifier: CA308471612

Gene: CYP2B6

Linked Data

• dbSNP Id: rs61365636
• gnomAD v2: 19-41524203-G-C
• gnomAD v3: 19-41018298-G-C
• gnomAD v4: 19-41018298-G-C
• MyVariant Identifiers: chr19:g.41524203G>C (hg19) ; chr19:g.41018298G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41018298G>C , CM000681.2:g.41018298G>C	GRCh38
NC_000019.9:g.41524203G>C , CM000681.1:g.41524203G>C	GRCh37
NC_000019.8:g.46216043G>C	NCBI36
NG_007929.1:g.32000G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.*1471G>C MANE Select	ENSP00000324648.2:n.*1471G>C
ENST00000324071.8:c.*1471G>C	ENSP00000324648.2:n.*1471G>C
NM_000767.4:c.*1471G>C	NP_000758.1:n.*1471G>C
XM_011526548.1:c.*1471G>C	XP_011524850.1:n.*1471G>C
XM_011526549.1:c.*1471G>C	XP_011524851.1:n.*1471G>C
XM_011526550.1:c.*1471G>C	XP_011524852.1:n.*1471G>C
NM_000767.5:c.*1471G>C MANE Select	NP_000758.1:n.*1471G>C