Canonical Allele Identifier: CA713592631
Gene: CYP19A1 HGNC NCBI
PIRC66 HGNC NCBI
MIR4713HG HGNC NCBI

Linked Data

dbSNP Id: rs1295534631

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.51257459C>A , CM000677.2:g.51257459C>A GRCh38
NC_000015.9:g.51549656C>A , CM000677.1:g.51549656C>A GRCh37
NC_000015.8:g.49336948C>A NCBI36
NG_007982.1:g.86140G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000396402.6:c.-38-14509G>T (CYP19A1) MANE Select ENSP00000379683.1:n.-38-14509G>T
ENST00000260433.6:c.-38-14509G>T (CYP19A1) ENSP00000260433.2:n.-38-14509G>T
ENST00000396402.5:c.-38-14509G>T (CYP19A1) ENSP00000379683.1:n.-38-14509G>T
ENST00000396404.8:c.-38-14509G>T (CYP19A1) ENSP00000379685.4:n.-38-14509G>T
ENST00000405011.6:c.-38-14509G>T (CYP19A1) ENSP00000384389.2:n.-38-14509G>T
ENST00000439712.6:c.-282-1698G>T (CYP19A1) ENSP00000390614.2:n.-282-1698G>T
ENST00000453807.6:c.-229-1751G>T (CYP19A1) ENSP00000391139.2:n.-229-1751G>T
ENST00000557858.5:c.-38-14509G>T (CYP19A1) ENSP00000452627.1:n.-38-14509G>T
ENST00000557934.5:c.-38-14509G>T (CYP19A1) ENSP00000454004.1:n.-38-14509G>T
ENST00000558328.5:c.-38-14509G>T (CYP19A1) ENSP00000453280.1:n.-38-14509G>T
ENST00000559646.1:c.-38-14509G>T (CYP19A1) ENSP00000453318.1:n.-38-14509G>T
ENST00000559980.5:c.-282-1698G>T (CYP19A1) ENSP00000452872.1:n.-282-1698G>T
ENST00000561075.5:c.-38-14509G>T (CYP19A1) ENSP00000454039.1:n.-38-14509G>T
NM_000103.3:c.-38-14509G>T (CYP19A1) NP_000094.2:n.-38-14509G>T
NM_031226.2:c.-38-14509G>T (CYP19A1) NP_112503.1:n.-38-14509G>T
XM_005254191.1:c.-38-14509G>T (CYP19A1) XP_005254248.1:n.-38-14509G>T
XR_932222.1:n.99-20524C>A (PIRC66)
NM_001347248.1:c.-38-14509G>T (CYP19A1) NP_001334177.1:n.-38-14509G>T
NM_001347249.1:c.-38-14509G>T (CYP19A1) NP_001334178.1:n.-38-14509G>T
NM_001347250.1:c.-38-14509G>T (CYP19A1) NP_001334179.1:n.-38-14509G>T
NM_001347251.1:c.-38-14509G>T (CYP19A1) NP_001334180.1:n.-38-14509G>T
NM_001347252.1:c.-38-14509G>T (CYP19A1) NP_001334181.1:n.-38-14509G>T
NR_146310.1:n.195-20524C>A (MIR4713HG)
NM_000103.4:c.-38-14509G>T (CYP19A1) MANE Select NP_000094.2:n.-38-14509G>T
NM_001347249.2:c.-38-14509G>T (CYP19A1) NP_001334178.1:n.-38-14509G>T
NM_031226.3:c.-38-14509G>T (CYP19A1) NP_112503.1:n.-38-14509G>T
NM_001347250.2:c.-38-14509G>T (CYP19A1) NP_001334179.1:n.-38-14509G>T
NM_001347251.2:c.-38-14509G>T (CYP19A1) NP_001334180.1:n.-38-14509G>T
NM_001347252.2:c.-38-14509G>T (CYP19A1) NP_001334181.1:n.-38-14509G>T