Canonical Allele Identifier: CA491489321
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75042208A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749867A>G , CM000677.2:g.74749867A>G GRCh38
NC_000015.9:g.75042208A>G , CM000677.1:g.75042208A>G GRCh37
NC_000015.8:g.72829261A>G NCBI36
NG_008431.1:g.32326A>G
NG_008431.2:g.32326A>G
NG_061543.1:g.6023A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.129A>G MANE Select ENSP00000342007.4:p.Pro43=
ENST00000343932.4:c.129A>G ENSP00000342007.4:p.Pro43=
NM_000761.4:c.129A>G NP_000752.2:p.Pro43=
NM_000761.5:c.129A>G MANE Select NP_000752.2:p.Pro43=