Canonical Allele Identifier: CA14080367
Gene: CYP19A1 HGNC NCBI
PIRC66 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2470152

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.51302775G>A , CM000677.2:g.51302775G>A GRCh38
NC_000015.9:g.51594972G>A , CM000677.1:g.51594972G>A GRCh37
NC_000015.8:g.49382264G>A NCBI36
NG_007982.1:g.40824C>T

Transcript Alleles

HGVS Amino-acid change
NM_000103.3:c.-39+35720C>T (CYP19A1) VV NP_000094.2:p.=
NM_031226.2:c.-39+21041C>T (CYP19A1) VV NP_112503.1:p.=
XM_005254191.1:c.-39+15658C>T (CYP19A1) XP_005254248.1:p.=
XR_932223.1:n.5100G>A (PIRC66)
XR_932229.1:n.5100G>A (PIRC66)
NM_001347248.1:c.-39+21041C>T (CYP19A1) VV NP_001334177.1:p.=
NM_001347249.1:c.-39+15658C>T (CYP19A1) VV NP_001334178.1:p.=
ENST00000260433.6:c.-39+21041C>T ENSP00000260433.2:p.=
ENST00000396402.5:c.-39+35720C>T ENSP00000379683.1:p.=
ENST00000396404.8:c.-39+21041C>T ENSP00000379685.4:p.=
ENST00000405011.6:c.-193-24613C>T ENSP00000384389.2:p.=
ENST00000439712.6:c.-283+35720C>T ENSP00000390614.2:p.=
ENST00000453807.6:c.-230+35720C>T ENSP00000391139.2:p.=
ENST00000557858.5:c.-39+35720C>T ENSP00000452627.1:p.=
ENST00000557934.5:c.-39+35720C>T ENSP00000454004.1:p.=
ENST00000558328.5:c.-39+35662C>T ENSP00000453280.1:p.=
ENST00000559646.1:c.-39+15658C>T ENSP00000453318.1:p.=
ENST00000559980.5:c.-283+35043C>T ENSP00000452872.1:p.=
ENST00000561075.5:c.-39+35720C>T ENSP00000454039.1:p.=