Canonical Allele Identifier: CA393179162
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75042606T>G (hg19) chr15:g.74750265T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750265T>G , CM000677.2:g.74750265T>G GRCh38
NC_000015.9:g.75042606T>G , CM000677.1:g.75042606T>G GRCh37
NC_000015.8:g.72829659T>G NCBI36
NG_008431.1:g.32724T>G
NG_008431.2:g.32724T>G
NG_061543.1:g.6421T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.527T>G MANE Select ENSP00000342007.4:p.Leu176Trp
ENST00000343932.4:c.527T>G ENSP00000342007.4:p.Leu176Trp
NM_000761.4:c.527T>G NP_000752.2:p.Leu176Trp
NM_000761.5:c.527T>G MANE Select NP_000752.2:p.Leu176Trp
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