Canonical Allele Identifier: CA270557511

Gene: CYP19A1 PIRC66

Linked Data

• dbSNP Id: rs28566535
• gnomAD v2: 15-51601141-A-G
• gnomAD v3: 15-51308944-A-G
• gnomAD v4: 15-51308944-A-G
• MyVariant Identifiers: chr15:g.51601141A>G (hg19) ; chr15:g.51308944A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51308944A>G , CM000677.2:g.51308944A>G	GRCh38
NC_000015.9:g.51601141A>G , CM000677.1:g.51601141A>G	GRCh37
NC_000015.8:g.49388433A>G	NCBI36
NG_007982.1:g.34655T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000396402.6:c.-39+29551T>C (CYP19A1) MANE Select	ENSP00000379683.1:n.-39+29551T>C
ENST00000260433.6:c.-39+14872T>C (CYP19A1)	ENSP00000260433.2:n.-39+14872T>C
ENST00000396402.5:c.-39+29551T>C (CYP19A1)	ENSP00000379683.1:n.-39+29551T>C
ENST00000396404.8:c.-39+14872T>C (CYP19A1)	ENSP00000379685.4:n.-39+14872T>C
ENST00000405011.6:c.-194+29551T>C (CYP19A1)	ENSP00000384389.2:n.-194+29551T>C
ENST00000439712.6:c.-283+29551T>C (CYP19A1)	ENSP00000390614.2:n.-283+29551T>C
ENST00000453807.6:c.-230+29551T>C (CYP19A1)	ENSP00000391139.2:n.-230+29551T>C
ENST00000557858.5:c.-39+29551T>C (CYP19A1)	ENSP00000452627.1:n.-39+29551T>C
ENST00000557934.5:c.-39+29551T>C (CYP19A1)	ENSP00000454004.1:n.-39+29551T>C
ENST00000558328.5:c.-39+29493T>C (CYP19A1)	ENSP00000453280.1:n.-39+29493T>C
ENST00000559646.1:c.-39+9489T>C (CYP19A1)	ENSP00000453318.1:n.-39+9489T>C
ENST00000559980.5:c.-283+28874T>C (CYP19A1)	ENSP00000452872.1:n.-283+28874T>C
ENST00000561075.5:c.-39+29551T>C (CYP19A1)	ENSP00000454039.1:n.-39+29551T>C
NM_000103.3:c.-39+29551T>C (CYP19A1)	NP_000094.2:n.-39+29551T>C
NM_031226.2:c.-39+14872T>C (CYP19A1)	NP_112503.1:n.-39+14872T>C
XM_005254191.1:c.-39+9489T>C (CYP19A1)	XP_005254248.1:n.-39+9489T>C
XR_932223.1:n.6645A>G (PIRC66)
XR_932224.1:n.3161A>G (PIRC66)
XR_932225.1:n.3161A>G (PIRC66)
XR_932226.1:n.2472-18A>G (PIRC66)
XR_932227.1:n.2472-18A>G (PIRC66)
XR_932229.1:n.5956-18A>G (PIRC66)
NM_001347248.1:c.-39+14872T>C (CYP19A1)	NP_001334177.1:n.-39+14872T>C
NM_001347249.1:c.-39+9489T>C (CYP19A1)	NP_001334178.1:n.-39+9489T>C
NM_000103.4:c.-39+29551T>C (CYP19A1) MANE Select	NP_000094.2:n.-39+29551T>C
NM_001347249.2:c.-39+9489T>C (CYP19A1)	NP_001334178.1:n.-39+9489T>C
NM_031226.3:c.-39+14872T>C (CYP19A1)	NP_112503.1:n.-39+14872T>C