Canonical Allele Identifier: CA2629503454
Gene: CYP1A1 HGNC NCBI

Linked Data

gnomAD v4: 15-74719897-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74719897A>T , CM000677.2:g.74719897A>T GRCh38
NC_000015.9:g.75012238A>T , CM000677.1:g.75012238A>T GRCh37
NC_000015.8:g.72799291A>T NCBI36
NG_008431.1:g.2356A>T
NG_008431.2:g.2356A>T
NG_061374.1:g.10632T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379727.8:c.*592T>A MANE Select ENSP00000369050.3:n.*592T>A
ENST00000379727.7:c.*592T>A ENSP00000369050.3:n.*592T>A
ENST00000395048.6:c.*592T>A ENSP00000378488.2:n.*592T>A
ENST00000612821.4:c.2047T>A ENSP00000479744.1:n.2047T>A
ENST00000617691.4:c.*592T>A ENSP00000482863.1:n.*592T>A
NM_000499.3:c.*592T>A NP_000490.1:n.*592T>A
XM_005254185.1:c.*592T>A XP_005254242.1:n.*592T>A
NM_000499.5:c.*592T>A NP_000490.1:n.*592T>A
NM_001319216.2:c.*592T>A NP_001306145.1:n.*592T>A
NM_001319217.2:c.*592T>A MANE Select NP_001306146.1:n.*592T>A
Search 100 bp 5'
Search 100 bp 3'