Canonical Allele Identifier: CA7660039
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs752138293
ExAC: 15:75045584 T / A
gnomAD v2: 15-75045584-T-A
gnomAD v4: 15-74753243-T-A
MyVariant Identifiers: chr15:g.75045584T>A (hg19) chr15:g.74753243T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74753243T>A , CM000677.2:g.74753243T>A GRCh38
NC_000015.9:g.75045584T>A , CM000677.1:g.75045584T>A GRCh37
NC_000015.8:g.72832637T>A NCBI36
NG_008431.1:g.35702T>A
NG_008431.2:g.35702T>A
NG_061543.1:g.9399T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1226T>A MANE Select ENSP00000342007.4:p.Val409Glu
ENST00000343932.4:c.1226T>A ENSP00000342007.4:p.Val409Glu
NM_000761.4:c.1226T>A NP_000752.2:p.Val409Glu
NM_000761.5:c.1226T>A MANE Select NP_000752.2:p.Val409Glu
Search 100 bp 5'
Search 100 bp 3'