Canonical Allele Identifier: CA393169572
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1373475971
gnomAD v2: 15-75047227-T-C
gnomAD v4: 15-74754886-T-C
MyVariant Identifiers: chr15:g.75047227T>C (hg19) chr15:g.74754886T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754886T>C , CM000677.2:g.74754886T>C GRCh38
NC_000015.9:g.75047227T>C , CM000677.1:g.75047227T>C GRCh37
NC_000015.8:g.72834280T>C NCBI36
NG_008431.1:g.37345T>C
NG_008431.2:g.37345T>C
NG_061543.1:g.11042T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1349T>C MANE Select ENSP00000342007.4:p.Leu450Pro
ENST00000343932.4:c.1349T>C ENSP00000342007.4:p.Leu450Pro
NM_000761.4:c.1349T>C NP_000752.2:p.Leu450Pro
NM_000761.5:c.1349T>C MANE Select NP_000752.2:p.Leu450Pro
Search 100 bp 5'
Search 100 bp 3'