Canonical Allele Identifier: CA393179335

Gene: CYP1A2

Linked Data

• MyVariant Identifiers: chr15:g.75042665G>A (hg19) ; chr15:g.74750324G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74750324G>A , CM000677.2:g.74750324G>A	GRCh38
NC_000015.9:g.75042665G>A , CM000677.1:g.75042665G>A	GRCh37
NC_000015.8:g.72829718G>A	NCBI36
NG_008431.1:g.32783G>A
NG_008431.2:g.32783G>A
NG_061543.1:g.6480G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.586G>A MANE Select	ENSP00000342007.4:p.Val196Met
ENST00000343932.4:c.586G>A	ENSP00000342007.4:p.Val196Met
NM_000761.4:c.586G>A	NP_000752.2:p.Val196Met
NM_000761.5:c.586G>A MANE Select	NP_000752.2:p.Val196Met