Canonical Allele Identifier: CA2629503421
Gene: CYP1A1 HGNC NCBI

Linked Data

gnomAD v4: 15-74719892-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74719892C>T , CM000677.2:g.74719892C>T GRCh38
NC_000015.9:g.75012233C>T , CM000677.1:g.75012233C>T GRCh37
NC_000015.8:g.72799286C>T NCBI36
NG_008431.1:g.2351C>T
NG_008431.2:g.2351C>T
NG_061374.1:g.10637G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379727.8:c.*597G>A MANE Select ENSP00000369050.3:n.*597G>A
ENST00000379727.7:c.*597G>A ENSP00000369050.3:n.*597G>A
ENST00000395048.6:c.*597G>A ENSP00000378488.2:n.*597G>A
ENST00000612821.4:c.2052G>A ENSP00000479744.1:n.2052G>A
ENST00000617691.4:c.*597G>A ENSP00000482863.1:n.*597G>A
NM_000499.3:c.*597G>A NP_000490.1:n.*597G>A
XM_005254185.1:c.*597G>A XP_005254242.1:n.*597G>A
NM_000499.5:c.*597G>A NP_000490.1:n.*597G>A
NM_001319216.2:c.*597G>A NP_001306145.1:n.*597G>A
NM_001319217.2:c.*597G>A MANE Select NP_001306146.1:n.*597G>A
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