Canonical Allele Identifier: CA2629512182
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74755334-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755334G>T , CM000677.2:g.74755334G>T GRCh38
NC_000015.9:g.75047675G>T , CM000677.1:g.75047675G>T GRCh37
NC_000015.8:g.72834728G>T NCBI36
NG_008431.1:g.37793G>T
NG_008431.2:g.37793G>T
NG_061543.1:g.11490G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*246G>T MANE Select ENSP00000342007.4:n.*246G>T
ENST00000343932.4:c.*246G>T ENSP00000342007.4:n.*246G>T
NM_000761.4:c.*246G>T NP_000752.2:n.*246G>T
NM_000761.5:c.*246G>T MANE Select NP_000752.2:n.*246G>T
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