Canonical Allele Identifier: CA491489332
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75042622A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750281A>G , CM000677.2:g.74750281A>G GRCh38
NC_000015.9:g.75042622A>G , CM000677.1:g.75042622A>G GRCh37
NC_000015.8:g.72829675A>G NCBI36
NG_008431.1:g.32740A>G
NG_008431.2:g.32740A>G
NG_061543.1:g.6437A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.543A>G MANE Select ENSP00000342007.4:p.Ala181=
ENST00000343932.4:c.543A>G ENSP00000342007.4:p.Ala181=
NM_000761.4:c.543A>G NP_000752.2:p.Ala181=
NM_000761.5:c.543A>G MANE Select NP_000752.2:p.Ala181=
Search 100 bp 5'
Search 100 bp 3'