Canonical Allele Identifier: CA619116664

Gene: CYP1A1

Linked Data

• dbSNP Id: rs1424812185
• gnomAD v2: 15-75012067-T-G
• MyVariant Identifiers: chr15:g.75012067T>G (hg19) ; chr15:g.74719726T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719726T>G , CM000677.2:g.74719726T>G	GRCh38
NC_000015.9:g.75012067T>G , CM000677.1:g.75012067T>G	GRCh37
NC_000015.8:g.72799120T>G	NCBI36
NG_008431.1:g.2185T>G
NG_008431.2:g.2185T>G
NG_061374.1:g.10803A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*763A>C MANE Select	ENSP00000369050.3:n.*763A>C
ENST00000379727.7:c.*763A>C	ENSP00000369050.3:n.*763A>C
ENST00000395048.6:c.*763A>C	ENSP00000378488.2:n.*763A>C
ENST00000612821.4:c.2218A>C	ENSP00000479744.1:n.2218A>C
ENST00000617691.4:c.*763A>C	ENSP00000482863.1:n.*763A>C
NM_000499.3:c.*763A>C	NP_000490.1:n.*763A>C
XM_005254185.1:c.*763A>C	XP_005254242.1:n.*763A>C
NM_000499.5:c.*763A>C	NP_000490.1:n.*763A>C
NM_001319216.2:c.*763A>C	NP_001306145.1:n.*763A>C
NM_001319217.2:c.*763A>C MANE Select	NP_001306146.1:n.*763A>C