Canonical Allele Identifier: CA393179032
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75042571T>A (hg19) chr15:g.74750230T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750230T>A , CM000677.2:g.74750230T>A GRCh38
NC_000015.9:g.75042571T>A , CM000677.1:g.75042571T>A GRCh37
NC_000015.8:g.72829624T>A NCBI36
NG_008431.1:g.32689T>A
NG_008431.2:g.32689T>A
NG_061543.1:g.6386T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.492T>A MANE Select ENSP00000342007.4:p.His164Gln
ENST00000343932.4:c.492T>A ENSP00000342007.4:p.His164Gln
NM_000761.4:c.492T>A NP_000752.2:p.His164Gln
NM_000761.5:c.492T>A MANE Select NP_000752.2:p.His164Gln
Search 100 bp 5'
Search 100 bp 3'