Canonical Allele Identifier: CA393176755
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749777G>T , CM000677.2:g.74749777G>T GRCh38
NC_000015.9:g.75042118G>T , CM000677.1:g.75042118G>T GRCh37
NC_000015.8:g.72829171G>T NCBI36
NG_008431.1:g.32236G>T
NG_008431.2:g.32236G>T
NG_061543.1:g.5933G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.39G>T MANE Select ENSP00000342007.4:p.Glu13Asp
ENST00000343932.4:c.39G>T ENSP00000342007.4:p.Glu13Asp
NM_000761.4:c.39G>T NP_000752.2:p.Glu13Asp
NM_000761.5:c.39G>T MANE Select NP_000752.2:p.Glu13Asp