Canonical Allele Identifier: CA216859203
Gene: CYP2E1 HGNC NCBI

Linked Data

dbSNP Id: rs919130855
gnomAD v4: 10-133539026-G-C
MyVariant Identifiers: chr10:g.135352530G>C (hg19) chr10:g.133539026G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133539026G>C , CM000672.2:g.133539026G>C GRCh38
NC_000010.10:g.135352530G>C , CM000672.1:g.135352530G>C GRCh37
NC_000010.9:g.135202520G>C NCBI36
NG_008383.1:g.16664G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252945.8:c.*62G>C MANE Select ENSP00000252945.3:n.*62G>C
ENST00000252945.7:c.*62G>C ENSP00000252945.3:n.*62G>C
ENST00000368520.1:n.1358+1134G>C
ENST00000463117.6:c.*62G>C ENSP00000440689.1:n.*62G>C
ENST00000469258.1:n.640G>C
NM_000773.3:c.*62G>C NP_000764.1:n.*62G>C
NM_000773.4:c.*62G>C MANE Select NP_000764.1:n.*62G>C
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