Canonical Allele Identifier: CA491488145

Gene: CYP1A1

Linked Data

• dbSNP Id: rs2141713563
• COSMIC: COSM3969273
• MyVariant Identifiers: chr15:g.75012968G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720627G>C , CM000677.2:g.74720627G>C	GRCh38
NC_000015.9:g.75012968G>C , CM000677.1:g.75012968G>C	GRCh37
NC_000015.8:g.72800021G>C	NCBI36
NG_008431.1:g.3086G>C
NG_008431.2:g.3086G>C
NG_061374.1:g.9902C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1401C>G MANE Select	ENSP00000369050.3:p.Val467=
ENST00000379727.7:c.1401C>G	ENSP00000369050.3:p.Val467=
ENST00000395048.6:c.1401C>G	ENSP00000378488.2:p.Val467=
ENST00000395049.8:c.1314C>G	ENSP00000378489.4:p.Val438=
ENST00000567032.5:c.1401C>G	ENSP00000456585.1:p.Val467=
ENST00000612821.4:c.1317C>G	ENSP00000479744.1:p.Val439=
ENST00000617691.4:c.1314C>G	ENSP00000482863.1:p.Val438=
NM_000499.3:c.1401C>G	NP_000490.1:p.Val467=
XM_005254185.1:c.1401C>G	XP_005254242.1:p.Val467=
NM_000499.5:c.1401C>G	NP_000490.1:p.Val467=
NM_001319216.2:c.1314C>G	NP_001306145.1:p.Val438=
NM_001319217.2:c.1401C>G MANE Select	NP_001306146.1:p.Val467=