Canonical Allele Identifier: CA2187827051
Gene: CYP1A2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754827G= , CM000677.2:g.74754827G= GRCh38
NC_000015.9:g.75047168G= , CM000677.1:g.75047168G= GRCh37
NC_000015.8:g.72834221G= NCBI36
NG_008431.1:g.37286G=
NG_008431.2:g.37286G=
NG_061543.1:g.10983G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1290G= MANE Select ENSP00000342007.4:p.Glu430=
ENST00000343932.4:c.1290G= ENSP00000342007.4:p.Glu430=
NM_000761.4:c.1290G= NP_000752.2:p.Glu430=
NM_000761.5:c.1290G= MANE Select NP_000752.2:p.Glu430=
Search 100 bp 5'
Search 100 bp 3'