Canonical Allele Identifier: CA491489182
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75042115A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749774A>T , CM000677.2:g.74749774A>T GRCh38
NC_000015.9:g.75042115A>T , CM000677.1:g.75042115A>T GRCh37
NC_000015.8:g.72829168A>T NCBI36
NG_008431.1:g.32233A>T
NG_008431.2:g.32233A>T
NG_061543.1:g.5930A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.36A>T MANE Select ENSP00000342007.4:p.Thr12=
ENST00000343932.4:c.36A>T ENSP00000342007.4:p.Thr12=
NM_000761.4:c.36A>T NP_000752.2:p.Thr12=
NM_000761.5:c.36A>T MANE Select NP_000752.2:p.Thr12=