Canonical Allele Identifier: CA7659937
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs369659890
ExAC: 15:75044151 T / C
gnomAD v2: 15-75044151-T-C
gnomAD v3: 15-74751810-T-C
gnomAD v4: 15-74751810-T-C
MyVariant Identifiers: chr15:g.75044151T>C (hg19) chr15:g.74751810T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751810T>C , CM000677.2:g.74751810T>C GRCh38
NC_000015.9:g.75044151T>C , CM000677.1:g.75044151T>C GRCh37
NC_000015.8:g.72831204T>C NCBI36
NG_008431.1:g.34269T>C
NG_008431.2:g.34269T>C
NG_061543.1:g.7966T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.998T>C MANE Select ENSP00000342007.4:p.Leu333Pro
ENST00000343932.4:c.998T>C ENSP00000342007.4:p.Leu333Pro
NM_000761.4:c.998T>C NP_000752.2:p.Leu333Pro
NM_000761.5:c.998T>C MANE Select NP_000752.2:p.Leu333Pro
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