Canonical Allele Identifier: CA393169604
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75047235A>C (hg19) chr15:g.74754894A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754894A>C , CM000677.2:g.74754894A>C GRCh38
NC_000015.9:g.75047235A>C , CM000677.1:g.75047235A>C GRCh37
NC_000015.8:g.72834288A>C NCBI36
NG_008431.1:g.37353A>C
NG_008431.2:g.37353A>C
NG_061543.1:g.11050A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1357A>C MANE Select ENSP00000342007.4:p.Met453Leu
ENST00000343932.4:c.1357A>C ENSP00000342007.4:p.Met453Leu
NM_000761.4:c.1357A>C NP_000752.2:p.Met453Leu
NM_000761.5:c.1357A>C MANE Select NP_000752.2:p.Met453Leu
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