Canonical Allele Identifier: CA2176808146

Gene: CYP19A1 PIRC66

Linked Data

• dbSNP Id: rs2036486978

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51319350A>G , CM000677.2:g.51319350A>G	GRCh38
NC_000015.9:g.51611547A>G , CM000677.1:g.51611547A>G	GRCh37
NC_000015.8:g.49398839A>G	NCBI36
NG_007982.1:g.24249T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396402.6:c.-39+19145T>C (CYP19A1) MANE Select	ENSP00000379683.1:n.-39+19145T>C
ENST00000260433.6:c.-39+4466T>C (CYP19A1)	ENSP00000260433.2:n.-39+4466T>C
ENST00000396402.5:c.-39+19145T>C (CYP19A1)	ENSP00000379683.1:n.-39+19145T>C
ENST00000396404.8:c.-39+4466T>C (CYP19A1)	ENSP00000379685.4:n.-39+4466T>C
ENST00000405011.6:c.-194+19145T>C (CYP19A1)	ENSP00000384389.2:n.-194+19145T>C
ENST00000439712.6:c.-283+19145T>C (CYP19A1)	ENSP00000390614.2:n.-283+19145T>C
ENST00000453807.6:c.-230+19145T>C (CYP19A1)	ENSP00000391139.2:n.-230+19145T>C
ENST00000492852.1:n.234-351T>C (CYP19A1)
ENST00000557858.5:c.-39+19145T>C (CYP19A1)	ENSP00000452627.1:n.-39+19145T>C
ENST00000557934.5:c.-39+19145T>C (CYP19A1)	ENSP00000454004.1:n.-39+19145T>C
ENST00000558328.5:c.-39+19087T>C (CYP19A1)	ENSP00000453280.1:n.-39+19087T>C
ENST00000559980.5:c.-283+18468T>C (CYP19A1)	ENSP00000452872.1:n.-283+18468T>C
ENST00000561075.5:c.-39+19145T>C (CYP19A1)	ENSP00000454039.1:n.-39+19145T>C
NM_000103.3:c.-39+19145T>C (CYP19A1)	NP_000094.2:n.-39+19145T>C
NM_031226.2:c.-39+4466T>C (CYP19A1)	NP_112503.1:n.-39+4466T>C
XR_932224.1:n.3218-1599A>G (PIRC66)
XR_932226.1:n.2511-1599A>G (PIRC66)
XR_932229.1:n.5995-1599A>G (PIRC66)
XR_932230.1:n.294-1599A>G (PIRC66)
NM_001347248.1:c.-39+4466T>C (CYP19A1)	NP_001334177.1:n.-39+4466T>C
NM_000103.4:c.-39+19145T>C (CYP19A1) MANE Select	NP_000094.2:n.-39+19145T>C
NM_031226.3:c.-39+4466T>C (CYP19A1)	NP_112503.1:n.-39+4466T>C