Canonical Allele Identifier: CA393169697
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75047254T>G (hg19) chr15:g.74754913T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754913T>G , CM000677.2:g.74754913T>G GRCh38
NC_000015.9:g.75047254T>G , CM000677.1:g.75047254T>G GRCh37
NC_000015.8:g.72834307T>G NCBI36
NG_008431.1:g.37372T>G
NG_008431.2:g.37372T>G
NG_061543.1:g.11069T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1376T>G MANE Select ENSP00000342007.4:p.Ile459Ser
ENST00000343932.4:c.1376T>G ENSP00000342007.4:p.Ile459Ser
NM_000761.4:c.1376T>G NP_000752.2:p.Ile459Ser
NM_000761.5:c.1376T>G MANE Select NP_000752.2:p.Ile459Ser
Search 100 bp 5'
Search 100 bp 3'