Canonical Allele Identifier: CA491489653
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75047192T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754851T>A , CM000677.2:g.74754851T>A GRCh38
NC_000015.9:g.75047192T>A , CM000677.1:g.75047192T>A GRCh37
NC_000015.8:g.72834245T>A NCBI36
NG_008431.1:g.37310T>A
NG_008431.2:g.37310T>A
NG_061543.1:g.11007T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1314T>A MANE Select ENSP00000342007.4:p.Thr438=
ENST00000343932.4:c.1314T>A ENSP00000342007.4:p.Thr438=
NM_000761.4:c.1314T>A NP_000752.2:p.Thr438=
NM_000761.5:c.1314T>A MANE Select NP_000752.2:p.Thr438=