Canonical Allele Identifier: CA393179292
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750307A>T , CM000677.2:g.74750307A>T GRCh38
NC_000015.9:g.75042648A>T , CM000677.1:g.75042648A>T GRCh37
NC_000015.8:g.72829701A>T NCBI36
NG_008431.1:g.32766A>T
NG_008431.2:g.32766A>T
NG_061543.1:g.6463A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.569A>T MANE Select ENSP00000342007.4:p.Asn190Ile
ENST00000343932.4:c.569A>T ENSP00000342007.4:p.Asn190Ile
NM_000761.4:c.569A>T NP_000752.2:p.Asn190Ile
NM_000761.5:c.569A>T MANE Select NP_000752.2:p.Asn190Ile