Canonical Allele Identifier: CA2176800918

Gene: CYP19A1 PIRC66

Linked Data

• dbSNP Id: rs2036142988

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51302847C>T , CM000677.2:g.51302847C>T	GRCh38
NC_000015.9:g.51595044C>T , CM000677.1:g.51595044C>T	GRCh37
NC_000015.8:g.49382336C>T	NCBI36
NG_007982.1:g.40752G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396402.6:c.-39+35648G>A (CYP19A1) MANE Select	ENSP00000379683.1:n.-39+35648G>A
ENST00000260433.6:c.-39+20969G>A (CYP19A1)	ENSP00000260433.2:n.-39+20969G>A
ENST00000396402.5:c.-39+35648G>A (CYP19A1)	ENSP00000379683.1:n.-39+35648G>A
ENST00000396404.8:c.-39+20969G>A (CYP19A1)	ENSP00000379685.4:n.-39+20969G>A
ENST00000405011.6:c.-193-24685G>A (CYP19A1)	ENSP00000384389.2:n.-193-24685G>A
ENST00000439712.6:c.-283+35648G>A (CYP19A1)	ENSP00000390614.2:n.-283+35648G>A
ENST00000453807.6:c.-230+35648G>A (CYP19A1)	ENSP00000391139.2:n.-230+35648G>A
ENST00000557858.5:c.-39+35648G>A (CYP19A1)	ENSP00000452627.1:n.-39+35648G>A
ENST00000557934.5:c.-39+35648G>A (CYP19A1)	ENSP00000454004.1:n.-39+35648G>A
ENST00000558328.5:c.-39+35590G>A (CYP19A1)	ENSP00000453280.1:n.-39+35590G>A
ENST00000559646.1:c.-39+15586G>A (CYP19A1)	ENSP00000453318.1:n.-39+15586G>A
ENST00000559980.5:c.-283+34971G>A (CYP19A1)	ENSP00000452872.1:n.-283+34971G>A
ENST00000561075.5:c.-39+35648G>A (CYP19A1)	ENSP00000454039.1:n.-39+35648G>A
NM_000103.3:c.-39+35648G>A (CYP19A1)	NP_000094.2:n.-39+35648G>A
NM_031226.2:c.-39+20969G>A (CYP19A1)	NP_112503.1:n.-39+20969G>A
XM_005254191.1:c.-39+15586G>A (CYP19A1)	XP_005254248.1:n.-39+15586G>A
XR_932223.1:n.5172C>T (PIRC66)
XR_932229.1:n.5172C>T (PIRC66)
NM_001347248.1:c.-39+20969G>A (CYP19A1)	NP_001334177.1:n.-39+20969G>A
NM_001347249.1:c.-39+15586G>A (CYP19A1)	NP_001334178.1:n.-39+15586G>A
NM_000103.4:c.-39+35648G>A (CYP19A1) MANE Select	NP_000094.2:n.-39+35648G>A
NM_001347249.2:c.-39+15586G>A (CYP19A1)	NP_001334178.1:n.-39+15586G>A
NM_031226.3:c.-39+20969G>A (CYP19A1)	NP_112503.1:n.-39+20969G>A