Canonical Allele Identifier: CA633138129
Gene: CYP2B6 HGNC NCBI

Linked Data

dbSNP Id: rs1217765559
gnomAD v2: 19-41523915-G-C
gnomAD v3: 19-41018010-G-C
gnomAD v4: 19-41018010-G-C
MyVariant Identifiers: chr19:g.41523915G>C (hg19) chr19:g.41018010G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41018010G>C , CM000681.2:g.41018010G>C GRCh38
NC_000019.9:g.41523915G>C , CM000681.1:g.41523915G>C GRCh37
NC_000019.8:g.46215755G>C NCBI36
NG_007929.1:g.31712G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324071.10:c.*1183G>C MANE Select ENSP00000324648.2:n.*1183G>C
ENST00000324071.8:c.*1183G>C ENSP00000324648.2:n.*1183G>C
NM_000767.4:c.*1183G>C NP_000758.1:n.*1183G>C
XM_011526548.1:c.*1183G>C XP_011524850.1:n.*1183G>C
XM_011526549.1:c.*1183G>C XP_011524851.1:n.*1183G>C
XM_011526550.1:c.*1183G>C XP_011524852.1:n.*1183G>C
NM_000767.5:c.*1183G>C MANE Select NP_000758.1:n.*1183G>C
Search 100 bp 5'
Search 100 bp 3'