Canonical Allele Identifier: CA7660157
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs776042559
ExAC: 15:75047465 G / T
gnomAD v2: 15-75047465-G-T
gnomAD v3: 15-74755124-G-T
gnomAD v4: 15-74755124-G-T
MyVariant Identifiers: chr15:g.75047465G>T (hg19) chr15:g.74755124G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755124G>T , CM000677.2:g.74755124G>T GRCh38
NC_000015.9:g.75047465G>T , CM000677.1:g.75047465G>T GRCh37
NC_000015.8:g.72834518G>T NCBI36
NG_008431.1:g.37583G>T
NG_008431.2:g.37583G>T
NG_061543.1:g.11280G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*36G>T MANE Select ENSP00000342007.4:n.*36G>T
ENST00000343932.4:c.*36G>T ENSP00000342007.4:n.*36G>T
NM_000761.4:c.*36G>T NP_000752.2:n.*36G>T
NM_000761.5:c.*36G>T MANE Select NP_000752.2:n.*36G>T
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