Canonical Allele Identifier: CA393177392
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1378709714
gnomAD v2: 15-75042245-A-G
gnomAD v4: 15-74749904-A-G
MyVariant Identifiers: chr15:g.75042245A>G (hg19) chr15:g.74749904A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749904A>G , CM000677.2:g.74749904A>G GRCh38
NC_000015.9:g.75042245A>G , CM000677.1:g.75042245A>G GRCh37
NC_000015.8:g.72829298A>G NCBI36
NG_008431.1:g.32363A>G
NG_008431.2:g.32363A>G
NG_061543.1:g.6060A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.166A>G MANE Select ENSP00000342007.4:p.Thr56Ala
ENST00000343932.4:c.166A>G ENSP00000342007.4:p.Thr56Ala
NM_000761.4:c.166A>G NP_000752.2:p.Thr56Ala
NM_000761.5:c.166A>G MANE Select NP_000752.2:p.Thr56Ala
Search 100 bp 5'
Search 100 bp 3'