Canonical Allele Identifier: CA272815217
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs936553417
gnomAD v4: 15-74751950-A-T
MyVariant Identifiers: chr15:g.75044291A>T (hg19) chr15:g.74751950A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751950A>T , CM000677.2:g.74751950A>T GRCh38
NC_000015.9:g.75044291A>T , CM000677.1:g.75044291A>T GRCh37
NC_000015.8:g.72831344A>T NCBI36
NG_008431.1:g.34409A>T
NG_008431.2:g.34409A>T
NG_061543.1:g.8106A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1042+96A>T MANE Select ENSP00000342007.4:n.1042+96A>T
ENST00000343932.4:c.1042+96A>T ENSP00000342007.4:n.1042+96A>T
NM_000761.4:c.1042+96A>T NP_000752.2:n.1042+96A>T
NM_000761.5:c.1042+96A>T MANE Select NP_000752.2:n.1042+96A>T
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