Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51210789G>T , CM000677.2:g.51210789G>T	GRCh38
NC_000015.9:g.51502986G>T , CM000677.1:g.51502986G>T	GRCh37
NC_000015.8:g.49290278G>T	NCBI36
NG_007982.1:g.132810C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000103.4:c.*19C>A (CYP19A1) MANE Select	NP_000094.2:n.*19C>A
ENST00000396402.6:c.*19C>A (CYP19A1) MANE Select	ENSP00000379683.1:n.*19C>A
NM_000103.3:c.*19C>A (CYP19A1)	NP_000094.2:n.*19C>A
NM_001347248.1:c.*19C>A (CYP19A1)	NP_001334177.1:n.*19C>A
NM_001347249.1:c.*19C>A (CYP19A1)	NP_001334178.1:n.*19C>A
NM_001347249.2:c.*19C>A (CYP19A1)	NP_001334178.1:n.*19C>A
NM_001347250.1:c.*19C>A (CYP19A1)	NP_001334179.1:n.*19C>A
NM_001347250.2:c.*19C>A (CYP19A1)	NP_001334179.1:n.*19C>A
NM_001347251.1:c.*19C>A (CYP19A1)	NP_001334180.1:n.*19C>A
NM_001347251.2:c.*19C>A (CYP19A1)	NP_001334180.1:n.*19C>A
NM_001347252.1:c.*19C>A (CYP19A1)	NP_001334181.1:n.*19C>A
NM_001347252.2:c.*19C>A (CYP19A1)	NP_001334181.1:n.*19C>A
NM_001347253.1:c.*19C>A (CYP19A1)	NP_001334182.1:n.*19C>A
NM_001347253.2:c.*19C>A (CYP19A1)	NP_001334182.1:n.*19C>A
NM_001347254.1:c.*19C>A (CYP19A1)	NP_001334183.1:n.*19C>A
NM_001347254.2:c.*19C>A (CYP19A1)	NP_001334183.1:n.*19C>A
NM_001347255.1:c.*19C>A (CYP19A1)	NP_001334184.1:n.*19C>A
NM_001347255.2:c.*19C>A (CYP19A1)	NP_001334184.1:n.*19C>A
NM_001347256.1:c.*19C>A (CYP19A1)	NP_001334185.1:n.*19C>A
NM_001347256.2:c.*19C>A (CYP19A1)	NP_001334185.1:n.*19C>A
NM_031226.2:c.*19C>A (CYP19A1)	NP_112503.1:n.*19C>A
NM_031226.3:c.*19C>A (CYP19A1)	NP_112503.1:n.*19C>A
NR_146310.1:n.195-67194G>T (MIR4713HG)
ENST00000260433.6:c.*19C>A (CYP19A1)	ENSP00000260433.2:n.*19C>A
ENST00000396402.5:c.*19C>A (CYP19A1)	ENSP00000379683.1:n.*19C>A
ENST00000396404.8:c.*19C>A (CYP19A1)	ENSP00000379685.4:n.*19C>A
ENST00000559878.5:c.*19C>A (CYP19A1)	ENSP00000453149.1:n.*19C>A
XM_005254190.1:c.*19C>A (CYP19A1)	XP_005254247.1:n.*19C>A
XM_005254191.1:c.*19C>A (CYP19A1)	XP_005254248.1:n.*19C>A
XR_932222.1:n.99-67194G>T (PIRC66)