Canonical Allele Identifier: CA392426215

Gene: CYP19A1 PIRC66 MIR4713HG

Linked Data

• dbSNP Id: rs2032165577
• gnomAD v4: 15-51222334-T-C
• MyVariant Identifiers: chr15:g.51514531T>C (hg19) ; chr15:g.51222334T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51222334T>C , CM000677.2:g.51222334T>C	GRCh38
NC_000015.9:g.51514531T>C , CM000677.1:g.51514531T>C	GRCh37
NC_000015.8:g.49301823T>C	NCBI36
NG_007982.1:g.121265A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396402.6:c.628+15A>G (CYP19A1) MANE Select	ENSP00000379683.1:n.628+15A>G
ENST00000260433.6:c.628+15A>G (CYP19A1)	ENSP00000260433.2:n.628+15A>G
ENST00000396402.5:c.628+15A>G (CYP19A1)	ENSP00000379683.1:n.628+15A>G
ENST00000396404.8:c.628+15A>G (CYP19A1)	ENSP00000379685.4:n.628+15A>G
ENST00000405913.7:c.643A>G (CYP19A1)	ENSP00000383930.3:p.Thr215Ala
ENST00000439712.6:c.628+15A>G (CYP19A1)	ENSP00000390614.2:n.628+15A>G
ENST00000453807.6:c.628+15A>G (CYP19A1)	ENSP00000391139.2:n.628+15A>G
ENST00000557858.5:c.643A>G (CYP19A1)	ENSP00000452627.1:p.Thr215Ala
ENST00000557934.5:c.628+15A>G (CYP19A1)	ENSP00000454004.1:n.628+15A>G
ENST00000558066.1:n.6+15A>G (CYP19A1)
ENST00000558328.5:c.628+15A>G (CYP19A1)	ENSP00000453280.1:n.628+15A>G
ENST00000559878.5:c.628+15A>G (CYP19A1)	ENSP00000453149.1:n.628+15A>G
ENST00000561075.5:c.452-3679A>G (CYP19A1)	ENSP00000454039.1:n.452-3679A>G
NM_000103.3:c.628+15A>G (CYP19A1)	NP_000094.2:n.628+15A>G
NM_031226.2:c.628+15A>G (CYP19A1)	NP_112503.1:n.628+15A>G
XM_005254190.1:c.628+15A>G (CYP19A1)	XP_005254247.1:n.628+15A>G
XM_005254191.1:c.628+15A>G (CYP19A1)	XP_005254248.1:n.628+15A>G
XR_932222.1:n.99-55649T>C (PIRC66)
NM_001347248.1:c.628+15A>G (CYP19A1)	NP_001334177.1:n.628+15A>G
NM_001347249.1:c.628+15A>G (CYP19A1)	NP_001334178.1:n.628+15A>G
NM_001347250.1:c.628+15A>G (CYP19A1)	NP_001334179.1:n.628+15A>G
NM_001347251.1:c.628+15A>G (CYP19A1)	NP_001334180.1:n.628+15A>G
NM_001347252.1:c.628+15A>G (CYP19A1)	NP_001334181.1:n.628+15A>G
NM_001347253.1:c.628+15A>G (CYP19A1)	NP_001334182.1:n.628+15A>G
NM_001347254.1:c.628+15A>G (CYP19A1)	NP_001334183.1:n.628+15A>G
NM_001347255.1:c.628+15A>G (CYP19A1)	NP_001334184.1:n.628+15A>G
NM_001347256.1:c.628+15A>G (CYP19A1)	NP_001334185.1:n.628+15A>G
NR_146310.1:n.195-55649T>C (MIR4713HG)
NM_000103.4:c.628+15A>G (CYP19A1) MANE Select	NP_000094.2:n.628+15A>G
NM_001347249.2:c.628+15A>G (CYP19A1)	NP_001334178.1:n.628+15A>G
NM_001347255.2:c.628+15A>G (CYP19A1)	NP_001334184.1:n.628+15A>G
NM_001347256.2:c.628+15A>G (CYP19A1)	NP_001334185.1:n.628+15A>G
NM_031226.3:c.628+15A>G (CYP19A1)	NP_112503.1:n.628+15A>G
NM_001347250.2:c.628+15A>G (CYP19A1)	NP_001334179.1:n.628+15A>G
NM_001347251.2:c.628+15A>G (CYP19A1)	NP_001334180.1:n.628+15A>G
NM_001347252.2:c.628+15A>G (CYP19A1)	NP_001334181.1:n.628+15A>G
NM_001347253.2:c.628+15A>G (CYP19A1)	NP_001334182.1:n.628+15A>G
NM_001347254.2:c.628+15A>G (CYP19A1)	NP_001334183.1:n.628+15A>G