Canonical Allele Identifier: CA7559991

Gene: CYP19A1 PIRC66 MIR4713HG

Linked Data

• ClinVar Variation Id: 316475
• ClinVar RCV Id: RCV000387706 ; RCV001452143
• dbSNP Id: rs781489846
• ExAC: 15:51510862 A / G
• gnomAD v2: 15-51510862-A-G
• gnomAD v3: 15-51218665-A-G
• gnomAD v4: 15-51218665-A-G
• MyVariant Identifiers: chr15:g.51510862A>G (hg19) ; chr15:g.51218665A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51218665A>G , CM000677.2:g.51218665A>G	GRCh38
NC_000015.9:g.51510862A>G , CM000677.1:g.51510862A>G	GRCh37
NC_000015.8:g.49298154A>G	NCBI36
NG_007982.1:g.124934T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396402.6:c.629-10T>C (CYP19A1) MANE Select	ENSP00000379683.1:n.629-10T>C
ENST00000260433.6:c.629-10T>C (CYP19A1)	ENSP00000260433.2:n.629-10T>C
ENST00000396402.5:c.629-10T>C (CYP19A1)	ENSP00000379683.1:n.629-10T>C
ENST00000396404.8:c.629-10T>C (CYP19A1)	ENSP00000379685.4:n.629-10T>C
ENST00000439712.6:c.629-10T>C (CYP19A1)	ENSP00000390614.2:n.629-10T>C
ENST00000453807.6:c.629-10T>C (CYP19A1)	ENSP00000391139.2:n.629-10T>C
ENST00000557934.5:c.629-10T>C (CYP19A1)	ENSP00000454004.1:n.629-10T>C
ENST00000558066.1:n.7-10T>C (CYP19A1)
ENST00000558328.5:c.629-10T>C (CYP19A1)	ENSP00000453280.1:n.629-10T>C
ENST00000559878.5:c.629-10T>C (CYP19A1)	ENSP00000453149.1:n.629-10T>C
ENST00000561075.5:c.452-10T>C (CYP19A1)	ENSP00000454039.1:n.452-10T>C
NM_000103.3:c.629-10T>C (CYP19A1)	NP_000094.2:n.629-10T>C
NM_031226.2:c.629-10T>C (CYP19A1)	NP_112503.1:n.629-10T>C
XM_005254190.1:c.629-10T>C (CYP19A1)	XP_005254247.1:n.629-10T>C
XM_005254191.1:c.629-10T>C (CYP19A1)	XP_005254248.1:n.629-10T>C
XR_932222.1:n.99-59318A>G (PIRC66)
NM_001347248.1:c.629-10T>C (CYP19A1)	NP_001334177.1:n.629-10T>C
NM_001347249.1:c.629-10T>C (CYP19A1)	NP_001334178.1:n.629-10T>C
NM_001347250.1:c.629-10T>C (CYP19A1)	NP_001334179.1:n.629-10T>C
NM_001347251.1:c.629-10T>C (CYP19A1)	NP_001334180.1:n.629-10T>C
NM_001347252.1:c.629-10T>C (CYP19A1)	NP_001334181.1:n.629-10T>C
NM_001347253.1:c.629-10T>C (CYP19A1)	NP_001334182.1:n.629-10T>C
NM_001347254.1:c.629-10T>C (CYP19A1)	NP_001334183.1:n.629-10T>C
NM_001347255.1:c.629-10T>C (CYP19A1)	NP_001334184.1:n.629-10T>C
NM_001347256.1:c.629-10T>C (CYP19A1)	NP_001334185.1:n.629-10T>C
NR_146310.1:n.195-59318A>G (MIR4713HG)
NM_000103.4:c.629-10T>C (CYP19A1) MANE Select	NP_000094.2:n.629-10T>C
NM_001347249.2:c.629-10T>C (CYP19A1)	NP_001334178.1:n.629-10T>C
NM_001347255.2:c.629-10T>C (CYP19A1)	NP_001334184.1:n.629-10T>C
NM_001347256.2:c.629-10T>C (CYP19A1)	NP_001334185.1:n.629-10T>C
NM_031226.3:c.629-10T>C (CYP19A1)	NP_112503.1:n.629-10T>C
NM_001347250.2:c.629-10T>C (CYP19A1)	NP_001334179.1:n.629-10T>C
NM_001347251.2:c.629-10T>C (CYP19A1)	NP_001334180.1:n.629-10T>C
NM_001347252.2:c.629-10T>C (CYP19A1)	NP_001334181.1:n.629-10T>C
NM_001347253.2:c.629-10T>C (CYP19A1)	NP_001334182.1:n.629-10T>C
NM_001347254.2:c.629-10T>C (CYP19A1)	NP_001334183.1:n.629-10T>C