Linked Data
ClinVar Variation Id:
316476
dbSNP Id:
rs28757184
ExAC:
15:51514572 G / A
gnomAD v2:
15-51514572-G-A
gnomAD v3:
15-51222375-G-A
gnomAD v4:
15-51222375-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.51222375G>A , CM000677.2:g.51222375G>A | GRCh38 |
| NC_000015.9:g.51514572G>A , CM000677.1:g.51514572G>A | GRCh37 |
| NC_000015.8:g.49301864G>A | NCBI36 |
| NG_007982.1:g.121224C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000396402.6:c.602C>T (CYP19A1) MANE Select | ENSP00000379683.1:p.Thr201Met | |
| ENST00000260433.6:c.602C>T (CYP19A1) | ENSP00000260433.2:p.Thr201Met | |
| ENST00000396402.5:c.602C>T (CYP19A1) | ENSP00000379683.1:p.Thr201Met | |
| ENST00000396404.8:c.602C>T (CYP19A1) | ENSP00000379685.4:p.Thr201Met | |
| ENST00000405913.7:c.602C>T (CYP19A1) | ENSP00000383930.3:p.Thr201Met | |
| ENST00000439712.6:c.602C>T (CYP19A1) | ENSP00000390614.2:p.Thr201Met | |
| ENST00000453807.6:c.602C>T (CYP19A1) | ENSP00000391139.2:p.Thr201Met | |
| ENST00000557858.5:c.602C>T (CYP19A1) | ENSP00000452627.1:p.Thr201Met | |
| ENST00000557934.5:c.602C>T (CYP19A1) | ENSP00000454004.1:p.Thr201Met | |
| ENST00000558328.5:c.602C>T (CYP19A1) | ENSP00000453280.1:p.Thr201Met | |
| ENST00000559878.5:c.602C>T (CYP19A1) | ENSP00000453149.1:p.Thr201Met | |
| ENST00000561075.5:c.452-3720C>T (CYP19A1) | ENSP00000454039.1:n.452-3720C>T | |
| NM_000103.3:c.602C>T (CYP19A1) | NP_000094.2:p.Thr201Met | |
| NM_031226.2:c.602C>T (CYP19A1) | NP_112503.1:p.Thr201Met | |
| XM_005254190.1:c.602C>T (CYP19A1) | XP_005254247.1:p.Thr201Met | |
| XM_005254191.1:c.602C>T (CYP19A1) | XP_005254248.1:p.Thr201Met | |
| XR_932222.1:n.99-55608G>A (PIRC66) | ||
| NM_001347248.1:c.602C>T (CYP19A1) | NP_001334177.1:p.Thr201Met | |
| NM_001347249.1:c.602C>T (CYP19A1) | NP_001334178.1:p.Thr201Met | |
| NM_001347250.1:c.602C>T (CYP19A1) | NP_001334179.1:p.Thr201Met | |
| NM_001347251.1:c.602C>T (CYP19A1) | NP_001334180.1:p.Thr201Met | |
| NM_001347252.1:c.602C>T (CYP19A1) | NP_001334181.1:p.Thr201Met | |
| NM_001347253.1:c.602C>T (CYP19A1) | NP_001334182.1:p.Thr201Met | |
| NM_001347254.1:c.602C>T (CYP19A1) | NP_001334183.1:p.Thr201Met | |
| NM_001347255.1:c.602C>T (CYP19A1) | NP_001334184.1:p.Thr201Met | |
| NM_001347256.1:c.602C>T (CYP19A1) | NP_001334185.1:p.Thr201Met | |
| NR_146310.1:n.195-55608G>A (MIR4713HG) | ||
| NM_000103.4:c.602C>T (CYP19A1) MANE Select | NP_000094.2:p.Thr201Met | |
| NM_001347249.2:c.602C>T (CYP19A1) | NP_001334178.1:p.Thr201Met | |
| NM_001347255.2:c.602C>T (CYP19A1) | NP_001334184.1:p.Thr201Met | |
| NM_001347256.2:c.602C>T (CYP19A1) | NP_001334185.1:p.Thr201Met | |
| NM_031226.3:c.602C>T (CYP19A1) | NP_112503.1:p.Thr201Met | |
| NM_001347250.2:c.602C>T (CYP19A1) | NP_001334179.1:p.Thr201Met | |
| NM_001347251.2:c.602C>T (CYP19A1) | NP_001334180.1:p.Thr201Met | |
| NM_001347252.2:c.602C>T (CYP19A1) | NP_001334181.1:p.Thr201Met | |
| NM_001347253.2:c.602C>T (CYP19A1) | NP_001334182.1:p.Thr201Met | |
| NM_001347254.2:c.602C>T (CYP19A1) | NP_001334183.1:p.Thr201Met |