Canonical Allele Identifier: CA393169660

Gene: CYP1A2

Linked Data

• MyVariant Identifiers: chr15:g.75047245G>T (hg19) ; chr15:g.74754904G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74754904G>T , CM000677.2:g.74754904G>T	GRCh38
NC_000015.9:g.75047245G>T , CM000677.1:g.75047245G>T	GRCh37
NC_000015.8:g.72834298G>T	NCBI36
NG_008431.1:g.37363G>T
NG_008431.2:g.37363G>T
NG_061543.1:g.11060G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.1367G>T MANE Select	ENSP00000342007.4:p.Arg456Leu
ENST00000343932.4:c.1367G>T	ENSP00000342007.4:p.Arg456Leu
NM_000761.4:c.1367G>T	NP_000752.2:p.Arg456Leu
NM_000761.5:c.1367G>T MANE Select	NP_000752.2:p.Arg456Leu