Canonical Allele Identifier: CA2629509374
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74751920-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751920A>C , CM000677.2:g.74751920A>C GRCh38
NC_000015.9:g.75044261A>C , CM000677.1:g.75044261A>C GRCh37
NC_000015.8:g.72831314A>C NCBI36
NG_008431.1:g.34379A>C
NG_008431.2:g.34379A>C
NG_061543.1:g.8076A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1042+66A>C MANE Select ENSP00000342007.4:n.1042+66A>C
ENST00000343932.4:c.1042+66A>C ENSP00000342007.4:n.1042+66A>C
NM_000761.4:c.1042+66A>C NP_000752.2:n.1042+66A>C
NM_000761.5:c.1042+66A>C MANE Select NP_000752.2:n.1042+66A>C
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