Canonical Allele Identifier: CA7559758
Gene: CYP19A1 HGNC NCBI
PIRC66 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 316469
ClinVar RCV Id: RCV000323501
dbSNP Id: rs10046

User contributed link-outs

Genomic Alleles

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

Transcript Alleles

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