Canonical Allele Identifier: CA272815183
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs995673317
gnomAD v3: 15-74751805-G-A
gnomAD v4: 15-74751805-G-A
MyVariant Identifiers: chr15:g.75044146G>A (hg19) chr15:g.74751805G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751805G>A , CM000677.2:g.74751805G>A GRCh38
NC_000015.9:g.75044146G>A , CM000677.1:g.75044146G>A GRCh37
NC_000015.8:g.72831199G>A NCBI36
NG_008431.1:g.34264G>A
NG_008431.2:g.34264G>A
NG_061543.1:g.7961G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.993G>A MANE Select ENSP00000342007.4:p.Met331Ile
ENST00000343932.4:c.993G>A ENSP00000342007.4:p.Met331Ile
NM_000761.4:c.993G>A NP_000752.2:p.Met331Ile
NM_000761.5:c.993G>A MANE Select NP_000752.2:p.Met331Ile
Search 100 bp 5'
Search 100 bp 3'