Canonical Allele Identifier: CA393177506
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75042265C>G (hg19) chr15:g.74749924C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749924C>G , CM000677.2:g.74749924C>G GRCh38
NC_000015.9:g.75042265C>G , CM000677.1:g.75042265C>G GRCh37
NC_000015.8:g.72829318C>G NCBI36
NG_008431.1:g.32383C>G
NG_008431.2:g.32383C>G
NG_061543.1:g.6080C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.186C>G MANE Select ENSP00000342007.4:p.His62Gln
ENST00000343932.4:c.186C>G ENSP00000342007.4:p.His62Gln
NM_000761.4:c.186C>G NP_000752.2:p.His62Gln
NM_000761.5:c.186C>G MANE Select NP_000752.2:p.His62Gln
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Search 100 bp 3'