Canonical Allele Identifier: CA308471610
Gene: CYP2B6 HGNC NCBI

Linked Data

dbSNP Id: rs61365636
MyVariant Identifiers: chr19:g.41524203G>A (hg19) chr19:g.41018298G>A (hg38)
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Genomic Alleles

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

Transcript Alleles

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