Canonical Allele Identifier: CA491219648
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs2063316518
MyVariant Identifiers: chr15:g.75044143C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751802C>T , CM000677.2:g.74751802C>T GRCh38
NC_000015.9:g.75044143C>T , CM000677.1:g.75044143C>T GRCh37
NC_000015.8:g.72831196C>T NCBI36
NG_008431.1:g.34261C>T
NG_008431.2:g.34261C>T
NG_061543.1:g.7958C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.990C>T MANE Select ENSP00000342007.4:p.Leu330=
ENST00000343932.4:c.990C>T ENSP00000342007.4:p.Leu330=
NM_000761.4:c.990C>T NP_000752.2:p.Leu330=
NM_000761.5:c.990C>T MANE Select NP_000752.2:p.Leu330=
Search 100 bp 5'
Search 100 bp 3'