Canonical Allele Identifier: CA491489385
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75042466T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750125T>A , CM000677.2:g.74750125T>A GRCh38
NC_000015.9:g.75042466T>A , CM000677.1:g.75042466T>A GRCh37
NC_000015.8:g.72829519T>A NCBI36
NG_008431.1:g.32584T>A
NG_008431.2:g.32584T>A
NG_061543.1:g.6281T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.387T>A MANE Select ENSP00000342007.4:p.Ser129=
ENST00000343932.4:c.387T>A ENSP00000342007.4:p.Ser129=
NM_000761.4:c.387T>A NP_000752.2:p.Ser129=
NM_000761.5:c.387T>A MANE Select NP_000752.2:p.Ser129=
Search 100 bp 5'
Search 100 bp 3'