Canonical Allele Identifier: CA393177339
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749890T>G , CM000677.2:g.74749890T>G GRCh38
NC_000015.9:g.75042231T>G , CM000677.1:g.75042231T>G GRCh37
NC_000015.8:g.72829284T>G NCBI36
NG_008431.1:g.32349T>G
NG_008431.2:g.32349T>G
NG_061543.1:g.6046T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.152T>G MANE Select ENSP00000342007.4:p.Leu51Arg
ENST00000343932.4:c.152T>G ENSP00000342007.4:p.Leu51Arg
NM_000761.4:c.152T>G NP_000752.2:p.Leu51Arg
NM_000761.5:c.152T>G MANE Select NP_000752.2:p.Leu51Arg