Canonical Allele Identifier: CA272816051
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs969721209
gnomAD v2: 15-75047151-T-A
gnomAD v4: 15-74754810-T-A
MyVariant Identifiers: chr15:g.75047151T>A (hg19) chr15:g.74754810T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754810T>A , CM000677.2:g.74754810T>A GRCh38
NC_000015.9:g.75047151T>A , CM000677.1:g.75047151T>A GRCh37
NC_000015.8:g.72834204T>A NCBI36
NG_008431.1:g.37269T>A
NG_008431.2:g.37269T>A
NG_061543.1:g.10966T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1273T>A MANE Select ENSP00000342007.4:p.Ser425Thr
ENST00000343932.4:c.1273T>A ENSP00000342007.4:p.Ser425Thr
NM_000761.4:c.1273T>A NP_000752.2:p.Ser425Thr
NM_000761.5:c.1273T>A MANE Select NP_000752.2:p.Ser425Thr
Search 100 bp 5'
Search 100 bp 3'