Canonical Allele Identifier: CA491489333
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74750281-A-T
MyVariant Identifiers: chr15:g.75042622A>T (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.543A>T MANE Select ENSP00000342007.4:p.Ala181=
ENST00000343932.4:c.543A>T ENSP00000342007.4:p.Ala181=
NM_000761.4:c.543A>T NP_000752.2:p.Ala181=
NM_000761.5:c.543A>T MANE Select NP_000752.2:p.Ala181=
Search 100 bp 5'
Search 100 bp 3'