Linked Data
ClinVar Variation Id:
17823
ClinVar RCV Id:
RCV000019401
dbSNP Id:
rs786205110
PubMed:
PMID:12466340
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.51218658G>T , CM000677.2:g.51218658G>T | GRCh38 |
| NC_000015.9:g.51510855G>T , CM000677.1:g.51510855G>T | GRCh37 |
| NC_000015.8:g.49298147G>T | NCBI36 |
| NG_007982.1:g.124941C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396402.6:c.629-3C>A (CYP19A1) MANE Select | ENSP00000379683.1:n.629-3C>A | |
| ENST00000260433.6:c.629-3C>A (CYP19A1) | ENSP00000260433.2:n.629-3C>A | |
| ENST00000396402.5:c.629-3C>A (CYP19A1) | ENSP00000379683.1:n.629-3C>A | |
| ENST00000396404.8:c.629-3C>A (CYP19A1) | ENSP00000379685.4:n.629-3C>A | |
| ENST00000439712.6:c.629-3C>A (CYP19A1) | ENSP00000390614.2:n.629-3C>A | |
| ENST00000453807.6:c.629-3C>A (CYP19A1) | ENSP00000391139.2:n.629-3C>A | |
| ENST00000557934.5:c.629-3C>A (CYP19A1) | ENSP00000454004.1:n.629-3C>A | |
| ENST00000558066.1:n.7-3C>A (CYP19A1) | ||
| ENST00000558328.5:c.629-3C>A (CYP19A1) | ENSP00000453280.1:n.629-3C>A | |
| ENST00000559878.5:c.629-3C>A (CYP19A1) | ENSP00000453149.1:n.629-3C>A | |
| ENST00000561075.5:c.452-3C>A (CYP19A1) | ENSP00000454039.1:n.452-3C>A | |
| NM_000103.3:c.629-3C>A (CYP19A1) | NP_000094.2:n.629-3C>A | |
| NM_031226.2:c.629-3C>A (CYP19A1) | NP_112503.1:n.629-3C>A | |
| XM_005254190.1:c.629-3C>A (CYP19A1) | XP_005254247.1:n.629-3C>A | |
| XM_005254191.1:c.629-3C>A (CYP19A1) | XP_005254248.1:n.629-3C>A | |
| XR_932222.1:n.99-59325G>T (PIRC66) | ||
| NM_001347248.1:c.629-3C>A (CYP19A1) | NP_001334177.1:n.629-3C>A | |
| NM_001347249.1:c.629-3C>A (CYP19A1) | NP_001334178.1:n.629-3C>A | |
| NM_001347250.1:c.629-3C>A (CYP19A1) | NP_001334179.1:n.629-3C>A | |
| NM_001347251.1:c.629-3C>A (CYP19A1) | NP_001334180.1:n.629-3C>A | |
| NM_001347252.1:c.629-3C>A (CYP19A1) | NP_001334181.1:n.629-3C>A | |
| NM_001347253.1:c.629-3C>A (CYP19A1) | NP_001334182.1:n.629-3C>A | |
| NM_001347254.1:c.629-3C>A (CYP19A1) | NP_001334183.1:n.629-3C>A | |
| NM_001347255.1:c.629-3C>A (CYP19A1) | NP_001334184.1:n.629-3C>A | |
| NM_001347256.1:c.629-3C>A (CYP19A1) | NP_001334185.1:n.629-3C>A | |
| NR_146310.1:n.195-59325G>T (MIR4713HG) | ||
| NM_000103.4:c.629-3C>A (CYP19A1) MANE Select | NP_000094.2:n.629-3C>A | |
| NM_001347249.2:c.629-3C>A (CYP19A1) | NP_001334178.1:n.629-3C>A | |
| NM_001347255.2:c.629-3C>A (CYP19A1) | NP_001334184.1:n.629-3C>A | |
| NM_001347256.2:c.629-3C>A (CYP19A1) | NP_001334185.1:n.629-3C>A | |
| NM_031226.3:c.629-3C>A (CYP19A1) | NP_112503.1:n.629-3C>A | |
| NM_001347250.2:c.629-3C>A (CYP19A1) | NP_001334179.1:n.629-3C>A | |
| NM_001347251.2:c.629-3C>A (CYP19A1) | NP_001334180.1:n.629-3C>A | |
| NM_001347252.2:c.629-3C>A (CYP19A1) | NP_001334181.1:n.629-3C>A | |
| NM_001347253.2:c.629-3C>A (CYP19A1) | NP_001334182.1:n.629-3C>A | |
| NM_001347254.2:c.629-3C>A (CYP19A1) | NP_001334183.1:n.629-3C>A |