Canonical Allele Identifier: CA393177050
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75042171T>C (hg19) chr15:g.74749830T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749830T>C , CM000677.2:g.74749830T>C GRCh38
NC_000015.9:g.75042171T>C , CM000677.1:g.75042171T>C GRCh37
NC_000015.8:g.72829224T>C NCBI36
NG_008431.1:g.32289T>C
NG_008431.2:g.32289T>C
NG_061543.1:g.5986T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.92T>C MANE Select ENSP00000342007.4:p.Leu31Ser
ENST00000343932.4:c.92T>C ENSP00000342007.4:p.Leu31Ser
NM_000761.4:c.92T>C NP_000752.2:p.Leu31Ser
NM_000761.5:c.92T>C MANE Select NP_000752.2:p.Leu31Ser
Search 100 bp 5'
Search 100 bp 3'