Canonical Allele Identifier: CA393167928
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754798T>A , CM000677.2:g.74754798T>A GRCh38
NC_000015.9:g.75047139T>A , CM000677.1:g.75047139T>A GRCh37
NC_000015.8:g.72834192T>A NCBI36
NG_008431.1:g.37257T>A
NG_008431.2:g.37257T>A
NG_061543.1:g.10954T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1261T>A MANE Select ENSP00000342007.4:p.Trp421Arg
ENST00000343932.4:c.1261T>A ENSP00000342007.4:p.Trp421Arg
NM_000761.4:c.1261T>A NP_000752.2:p.Trp421Arg
NM_000761.5:c.1261T>A MANE Select NP_000752.2:p.Trp421Arg