Canonical Allele Identifier: CA270562300
Gene: CYP19A1 HGNC NCBI
PIRC66 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1902584

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.51319457A>T , CM000677.2:g.51319457A>T GRCh38
NC_000015.9:g.51611654A>T , CM000677.1:g.51611654A>T GRCh37
NC_000015.8:g.49398946A>T NCBI36
NG_007982.1:g.24142T>A

Transcript Alleles

HGVS Amino-acid change
NM_000103.3:c.-39+19038T>A (CYP19A1) VV NP_000094.2:p.=
NM_031226.2:c.-39+4359T>A (CYP19A1) VV NP_112503.1:p.=
XR_932224.1:n.3218-1492A>T (PIRC66)
XR_932226.1:n.2511-1492A>T (PIRC66)
XR_932229.1:n.5995-1492A>T (PIRC66)
XR_932230.1:n.294-1492A>T (PIRC66)
NM_001347248.1:c.-39+4359T>A (CYP19A1) VV NP_001334177.1:p.=
ENST00000260433.6:c.-39+4359T>A ENSP00000260433.2:p.=
ENST00000396402.5:c.-39+19038T>A ENSP00000379683.1:p.=
ENST00000396404.8:c.-39+4359T>A ENSP00000379685.4:p.=
ENST00000405011.6:c.-194+19038T>A ENSP00000384389.2:p.=
ENST00000439712.6:c.-283+19038T>A ENSP00000390614.2:p.=
ENST00000453807.6:c.-230+19038T>A ENSP00000391139.2:p.=
ENST00000492852.1:n.234-458T>A
ENST00000557858.5:c.-39+19038T>A ENSP00000452627.1:p.=
ENST00000557934.5:c.-39+19038T>A ENSP00000454004.1:p.=
ENST00000558328.5:c.-39+18980T>A ENSP00000453280.1:p.=
ENST00000559980.5:c.-283+18361T>A ENSP00000452872.1:p.=
ENST00000561075.5:c.-39+19038T>A ENSP00000454039.1:p.=