Canonical Allele Identifier: CA393164672
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75044169T>A (hg19) chr15:g.74751828T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751828T>A , CM000677.2:g.74751828T>A GRCh38
NC_000015.9:g.75044169T>A , CM000677.1:g.75044169T>A GRCh37
NC_000015.8:g.72831222T>A NCBI36
NG_008431.1:g.34287T>A
NG_008431.2:g.34287T>A
NG_061543.1:g.7984T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1016T>A MANE Select ENSP00000342007.4:p.Ile339Lys
ENST00000343932.4:c.1016T>A ENSP00000342007.4:p.Ile339Lys
NM_000761.4:c.1016T>A NP_000752.2:p.Ile339Lys
NM_000761.5:c.1016T>A MANE Select NP_000752.2:p.Ile339Lys
Search 100 bp 5'
Search 100 bp 3'