Canonical Allele Identifier: CA270549052

Gene: CYP19A1 PIRC66 MIR4713HG

Linked Data

• dbSNP Id: rs746052964
• MyVariant Identifiers: chr15:g.51549883T>C (hg19) ; chr15:g.51257686T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51257686T>C , CM000677.2:g.51257686T>C	GRCh38
NC_000015.9:g.51549883T>C , CM000677.1:g.51549883T>C	GRCh37
NC_000015.8:g.49337175T>C	NCBI36
NG_007982.1:g.85913A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396402.6:c.-38-14736A>G (CYP19A1) MANE Select	ENSP00000379683.1:n.-38-14736A>G
ENST00000260433.6:c.-38-14736A>G (CYP19A1)	ENSP00000260433.2:n.-38-14736A>G
ENST00000396402.5:c.-38-14736A>G (CYP19A1)	ENSP00000379683.1:n.-38-14736A>G
ENST00000396404.8:c.-38-14736A>G (CYP19A1)	ENSP00000379685.4:n.-38-14736A>G
ENST00000405011.6:c.-38-14736A>G (CYP19A1)	ENSP00000384389.2:n.-38-14736A>G
ENST00000439712.6:c.-282-1925A>G (CYP19A1)	ENSP00000390614.2:n.-282-1925A>G
ENST00000453807.6:c.-229-1978A>G (CYP19A1)	ENSP00000391139.2:n.-229-1978A>G
ENST00000557858.5:c.-38-14736A>G (CYP19A1)	ENSP00000452627.1:n.-38-14736A>G
ENST00000557934.5:c.-38-14736A>G (CYP19A1)	ENSP00000454004.1:n.-38-14736A>G
ENST00000558328.5:c.-38-14736A>G (CYP19A1)	ENSP00000453280.1:n.-38-14736A>G
ENST00000559646.1:c.-38-14736A>G (CYP19A1)	ENSP00000453318.1:n.-38-14736A>G
ENST00000559980.5:c.-282-1925A>G (CYP19A1)	ENSP00000452872.1:n.-282-1925A>G
ENST00000561075.5:c.-38-14736A>G (CYP19A1)	ENSP00000454039.1:n.-38-14736A>G
NM_000103.3:c.-38-14736A>G (CYP19A1)	NP_000094.2:n.-38-14736A>G
NM_031226.2:c.-38-14736A>G (CYP19A1)	NP_112503.1:n.-38-14736A>G
XM_005254191.1:c.-38-14736A>G (CYP19A1)	XP_005254248.1:n.-38-14736A>G
XR_932222.1:n.99-20297T>C (PIRC66)
NM_001347248.1:c.-38-14736A>G (CYP19A1)	NP_001334177.1:n.-38-14736A>G
NM_001347249.1:c.-38-14736A>G (CYP19A1)	NP_001334178.1:n.-38-14736A>G
NM_001347250.1:c.-38-14736A>G (CYP19A1)	NP_001334179.1:n.-38-14736A>G
NM_001347251.1:c.-38-14736A>G (CYP19A1)	NP_001334180.1:n.-38-14736A>G
NM_001347252.1:c.-38-14736A>G (CYP19A1)	NP_001334181.1:n.-38-14736A>G
NR_146310.1:n.195-20297T>C (MIR4713HG)
NM_000103.4:c.-38-14736A>G (CYP19A1) MANE Select	NP_000094.2:n.-38-14736A>G
NM_001347249.2:c.-38-14736A>G (CYP19A1)	NP_001334178.1:n.-38-14736A>G
NM_031226.3:c.-38-14736A>G (CYP19A1)	NP_112503.1:n.-38-14736A>G
NM_001347250.2:c.-38-14736A>G (CYP19A1)	NP_001334179.1:n.-38-14736A>G
NM_001347251.2:c.-38-14736A>G (CYP19A1)	NP_001334180.1:n.-38-14736A>G
NM_001347252.2:c.-38-14736A>G (CYP19A1)	NP_001334181.1:n.-38-14736A>G