Canonical Allele Identifier: CA393176998
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74749823-A-G
MyVariant Identifiers: chr15:g.75042164A>G (hg19) chr15:g.74749823A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749823A>G , CM000677.2:g.74749823A>G GRCh38
NC_000015.9:g.75042164A>G , CM000677.1:g.75042164A>G GRCh37
NC_000015.8:g.72829217A>G NCBI36
NG_008431.1:g.32282A>G
NG_008431.2:g.32282A>G
NG_061543.1:g.5979A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.85A>G MANE Select ENSP00000342007.4:p.Lys29Glu
ENST00000343932.4:c.85A>G ENSP00000342007.4:p.Lys29Glu
NM_000761.4:c.85A>G NP_000752.2:p.Lys29Glu
NM_000761.5:c.85A>G MANE Select NP_000752.2:p.Lys29Glu
Search 100 bp 5'
Search 100 bp 3'