Canonical Allele Identifier: CA393177190
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75042203C>A (hg19) chr15:g.74749862C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749862C>A , CM000677.2:g.74749862C>A GRCh38
NC_000015.9:g.75042203C>A , CM000677.1:g.75042203C>A GRCh37
NC_000015.8:g.72829256C>A NCBI36
NG_008431.1:g.32321C>A
NG_008431.2:g.32321C>A
NG_061543.1:g.6018C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.124C>A MANE Select ENSP00000342007.4:p.Pro42Thr
ENST00000343932.4:c.124C>A ENSP00000342007.4:p.Pro42Thr
NM_000761.4:c.124C>A NP_000752.2:p.Pro42Thr
NM_000761.5:c.124C>A MANE Select NP_000752.2:p.Pro42Thr
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Search 100 bp 3'