Canonical Allele Identifier: CA491489328
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75042214A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749873A>C , CM000677.2:g.74749873A>C GRCh38
NC_000015.9:g.75042214A>C , CM000677.1:g.75042214A>C GRCh37
NC_000015.8:g.72829267A>C NCBI36
NG_008431.1:g.32332A>C
NG_008431.2:g.32332A>C
NG_061543.1:g.6029A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.135A>C MANE Select ENSP00000342007.4:p.Pro45=
ENST00000343932.4:c.135A>C ENSP00000342007.4:p.Pro45=
NM_000761.4:c.135A>C NP_000752.2:p.Pro45=
NM_000761.5:c.135A>C MANE Select NP_000752.2:p.Pro45=