Canonical Allele Identifier: CA393176701
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749766T>A , CM000677.2:g.74749766T>A GRCh38
NC_000015.9:g.75042107T>A , CM000677.1:g.75042107T>A GRCh37
NC_000015.8:g.72829160T>A NCBI36
NG_008431.1:g.32225T>A
NG_008431.2:g.32225T>A
NG_061543.1:g.5922T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.28T>A MANE Select ENSP00000342007.4:p.Ser10Thr
ENST00000343932.4:c.28T>A ENSP00000342007.4:p.Ser10Thr
NM_000761.4:c.28T>A NP_000752.2:p.Ser10Thr
NM_000761.5:c.28T>A MANE Select NP_000752.2:p.Ser10Thr