Canonical Allele Identifier: CA2629503565
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74748958-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74748958A>G , CM000677.2:g.74748958A>G GRCh38
NC_000015.9:g.75041299A>G , CM000677.1:g.75041299A>G GRCh37
NC_000015.8:g.72828352A>G NCBI36
NG_008431.1:g.31417A>G
NG_008431.2:g.31417A>G
NG_061543.1:g.5114A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.-10+61A>G MANE Select ENSP00000342007.4:n.-10+61A>G
ENST00000343932.4:c.-10+61A>G ENSP00000342007.4:n.-10+61A>G
NM_000761.4:c.-10+61A>G NP_000752.2:n.-10+61A>G
NM_000761.5:c.-10+61A>G MANE Select NP_000752.2:n.-10+61A>G
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