Canonical Allele Identifier: CA491489342
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1596357594
MyVariant Identifiers: chr15:g.75042628T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750287T>C , CM000677.2:g.74750287T>C GRCh38
NC_000015.9:g.75042628T>C , CM000677.1:g.75042628T>C GRCh37
NC_000015.8:g.72829681T>C NCBI36
NG_008431.1:g.32746T>C
NG_008431.2:g.32746T>C
NG_061543.1:g.6443T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.549T>C MANE Select ENSP00000342007.4:p.Pro183=
ENST00000343932.4:c.549T>C ENSP00000342007.4:p.Pro183=
NM_000761.4:c.549T>C NP_000752.2:p.Pro183=
NM_000761.5:c.549T>C MANE Select NP_000752.2:p.Pro183=
Search 100 bp 5'
Search 100 bp 3'