Canonical Allele Identifier: CA491489666
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75047210G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754869G>A , CM000677.2:g.74754869G>A GRCh38
NC_000015.9:g.75047210G>A , CM000677.1:g.75047210G>A GRCh37
NC_000015.8:g.72834263G>A NCBI36
NG_008431.1:g.37328G>A
NG_008431.2:g.37328G>A
NG_061543.1:g.11025G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1332G>A MANE Select ENSP00000342007.4:p.Leu444=
ENST00000343932.4:c.1332G>A ENSP00000342007.4:p.Leu444=
NM_000761.4:c.1332G>A NP_000752.2:p.Leu444=
NM_000761.5:c.1332G>A MANE Select NP_000752.2:p.Leu444=