Canonical Allele Identifier: CA491489309
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1472783688
gnomAD v2: 15-75042607-G-A
gnomAD v3: 15-74750266-G-A
gnomAD v4: 15-74750266-G-A
MyVariant Identifiers: chr15:g.75042607G>A (hg19) chr15:g.74750266G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750266G>A , CM000677.2:g.74750266G>A GRCh38
NC_000015.9:g.75042607G>A , CM000677.1:g.75042607G>A GRCh37
NC_000015.8:g.72829660G>A NCBI36
NG_008431.1:g.32725G>A
NG_008431.2:g.32725G>A
NG_061543.1:g.6422G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.528G>A MANE Select ENSP00000342007.4:p.Leu176=
ENST00000343932.4:c.528G>A ENSP00000342007.4:p.Leu176=
NM_000761.4:c.528G>A NP_000752.2:p.Leu176=
NM_000761.5:c.528G>A MANE Select NP_000752.2:p.Leu176=
Search 100 bp 5'
Search 100 bp 3'