Canonical Allele Identifier: CA7659206

Gene: CYP1A1

Linked Data

• dbSNP Id: rs28399430
• ExAC: 15:75012894 G / C
• gnomAD v2: 15-75012894-G-C
• gnomAD v3: 15-74720553-G-C
• gnomAD v4: 15-74720553-G-C
• MyVariant Identifiers: chr15:g.75012894G>C (hg19) ; chr15:g.74720553G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720553G>C , CM000677.2:g.74720553G>C	GRCh38
NC_000015.9:g.75012894G>C , CM000677.1:g.75012894G>C	GRCh37
NC_000015.8:g.72799947G>C	NCBI36
NG_008431.1:g.3012G>C
NG_008431.2:g.3012G>C
NG_061374.1:g.9976C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000379727.8:c.1475C>G MANE Select	ENSP00000369050.3:p.Pro492Arg
ENST00000379727.7:c.1475C>G	ENSP00000369050.3:p.Pro492Arg
ENST00000395048.6:c.1475C>G	ENSP00000378488.2:p.Pro492Arg
ENST00000395049.8:c.1388C>G	ENSP00000378489.4:p.Pro463Arg
ENST00000567032.5:c.1475C>G	ENSP00000456585.1:p.Pro492Arg
ENST00000612821.4:c.1391C>G	ENSP00000479744.1:p.Pro464Arg
ENST00000617691.4:c.1388C>G	ENSP00000482863.1:p.Pro463Arg
NM_000499.3:c.1475C>G	NP_000490.1:p.Pro492Arg
XM_005254185.1:c.1475C>G	XP_005254242.1:p.Pro492Arg
NM_000499.5:c.1475C>G	NP_000490.1:p.Pro492Arg
NM_001319216.2:c.1388C>G	NP_001306145.1:p.Pro463Arg
NM_001319217.2:c.1475C>G MANE Select	NP_001306146.1:p.Pro492Arg