Canonical Allele Identifier: CA308471505
Gene: CYP2B6 HGNC NCBI

Linked Data

dbSNP Id: rs34031833
MyVariant Identifiers: chr19:g.41524126_41524127insC (hg19) chr19:g.41018221_41018222insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41018225dup , CM000681.2:g.41018225dup GRCh38
NC_000019.9:g.41524130dup , CM000681.1:g.41524130dup GRCh37
NC_000019.8:g.46215970dup NCBI36
NG_007929.1:g.31927dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.*1398dup MANE Select ENSP00000324648.2:n.*1398dup
ENST00000324071.8:c.*1398dup ENSP00000324648.2:n.*1398dup
NM_000767.4:c.*1398dup NP_000758.1:n.*1398dup
XM_011526548.1:c.*1398dup XP_011524850.1:n.*1398dup
XM_011526549.1:c.*1398dup XP_011524851.1:n.*1398dup
XM_011526550.1:c.*1398dup XP_011524852.1:n.*1398dup
NM_000767.5:c.*1398dup MANE Select NP_000758.1:n.*1398dup
Search 100 bp 5'
Search 100 bp 3'