Canonical Allele Identifier: CA15841094
Gene: CYP19A1 HGNC NCBI
PIRC66 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1004982

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.51321614T>C , CM000677.2:g.51321614T>C GRCh38
NC_000015.9:g.51613811T>C , CM000677.1:g.51613811T>C GRCh37
NC_000015.8:g.49401103T>C NCBI36
NG_007982.1:g.21985A>G

Transcript Alleles

HGVS Amino-acid change
NM_000103.3:c.-39+16881A>G (CYP19A1) VV NP_000094.2:p.=
NM_031226.2:c.-39+2202A>G (CYP19A1) VV NP_112503.1:p.=
XR_932224.1:n.3314T>C (PIRC66)
XR_932226.1:n.2607T>C (PIRC66)
XR_932229.1:n.6091T>C (PIRC66)
XR_932230.1:n.390T>C (PIRC66)
NM_001347248.1:c.-39+2202A>G (CYP19A1) VV NP_001334177.1:p.=
XR_002957708.1:n.370T>C
ENST00000260433.6:c.-39+2202A>G ENSP00000260433.2:p.=
ENST00000396402.5:c.-39+16881A>G ENSP00000379683.1:p.=
ENST00000396404.8:c.-39+2202A>G ENSP00000379685.4:p.=
ENST00000405011.6:c.-194+16881A>G ENSP00000384389.2:p.=
ENST00000439712.6:c.-283+16881A>G ENSP00000390614.2:p.=
ENST00000453807.6:c.-230+16881A>G ENSP00000391139.2:p.=
ENST00000492852.1:n.88-1241A>G
ENST00000557858.5:c.-39+16881A>G ENSP00000452627.1:p.=
ENST00000557934.5:c.-39+16881A>G ENSP00000454004.1:p.=
ENST00000558328.5:c.-39+16823A>G ENSP00000453280.1:p.=
ENST00000559980.5:c.-283+16204A>G ENSP00000452872.1:p.=
ENST00000561075.5:c.-39+16881A>G ENSP00000454039.1:p.=