Canonical Allele Identifier: CA715671196
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1462550715
gnomAD v3: 15-74755114-G-C
gnomAD v4: 15-74755114-G-C
MyVariant Identifiers: chr15:g.75047455G>C (hg19) chr15:g.74755114G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755114G>C , CM000677.2:g.74755114G>C GRCh38
NC_000015.9:g.75047455G>C , CM000677.1:g.75047455G>C GRCh37
NC_000015.8:g.72834508G>C NCBI36
NG_008431.1:g.37573G>C
NG_008431.2:g.37573G>C
NG_061543.1:g.11270G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*26G>C MANE Select ENSP00000342007.4:n.*26G>C
ENST00000343932.4:c.*26G>C ENSP00000342007.4:n.*26G>C
NM_000761.4:c.*26G>C NP_000752.2:n.*26G>C
NM_000761.5:c.*26G>C MANE Select NP_000752.2:n.*26G>C
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