Canonical Allele Identifier: CA393179163
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75042607G>C (hg19) chr15:g.74750266G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750266G>C , CM000677.2:g.74750266G>C GRCh38
NC_000015.9:g.75042607G>C , CM000677.1:g.75042607G>C GRCh37
NC_000015.8:g.72829660G>C NCBI36
NG_008431.1:g.32725G>C
NG_008431.2:g.32725G>C
NG_061543.1:g.6422G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.528G>C MANE Select ENSP00000342007.4:p.Leu176Phe
ENST00000343932.4:c.528G>C ENSP00000342007.4:p.Leu176Phe
NM_000761.4:c.528G>C NP_000752.2:p.Leu176Phe
NM_000761.5:c.528G>C MANE Select NP_000752.2:p.Leu176Phe
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