Canonical Allele Identifier: CA7659796
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs757272055

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750222G>A , CM000677.2:g.74750222G>A GRCh38
NC_000015.9:g.75042563G>A , CM000677.1:g.75042563G>A GRCh37
NC_000015.8:g.72829616G>A NCBI36
NG_008431.1:g.32681G>A
NG_008431.2:g.32681G>A
NG_061543.1:g.6378G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.484G>A MANE Select ENSP00000342007.4:p.Glu162Lys
ENST00000343932.4:c.484G>A ENSP00000342007.4:p.Glu162Lys
NM_000761.4:c.484G>A NP_000752.2:p.Glu162Lys
NM_000761.5:c.484G>A MANE Select NP_000752.2:p.Glu162Lys