Canonical Allele Identifier: CA272820067
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs35198905
gnomAD v3: 15-74749077-T-G
gnomAD v4: 15-74749077-T-G
MyVariant Identifiers: chr15:g.75041418T>G (hg19) chr15:g.74749077T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749077T>G , CM000677.2:g.74749077T>G GRCh38
NC_000015.9:g.75041418T>G , CM000677.1:g.75041418T>G GRCh37
NC_000015.8:g.72828471T>G NCBI36
NG_008431.1:g.31536T>G
NG_008431.2:g.31536T>G
NG_061543.1:g.5233T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.-10+180T>G MANE Select ENSP00000342007.4:n.-10+180T>G
ENST00000343932.4:c.-10+180T>G ENSP00000342007.4:n.-10+180T>G
NM_000761.4:c.-10+180T>G NP_000752.2:n.-10+180T>G
NM_000761.5:c.-10+180T>G MANE Select NP_000752.2:n.-10+180T>G
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