Linked Data
dbSNP Id:
rs936306
gnomAD v2:
15-51579598-C-T
gnomAD v3:
15-51287401-C-T
gnomAD v4:
15-51287401-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.51287401C>T , CM000677.2:g.51287401C>T | GRCh38 |
| NC_000015.9:g.51579598C>T , CM000677.1:g.51579598C>T | GRCh37 |
| NC_000015.8:g.49366890C>T | NCBI36 |
| NG_007982.1:g.56198G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000396402.6:c.-38-44451G>A (CYP19A1) MANE Select | ENSP00000379683.1:n.-38-44451G>A | |
| ENST00000260433.6:c.-39+36415G>A (CYP19A1) | ENSP00000260433.2:n.-39+36415G>A | |
| ENST00000396402.5:c.-38-44451G>A (CYP19A1) | ENSP00000379683.1:n.-38-44451G>A | |
| ENST00000396404.8:c.-39+36415G>A (CYP19A1) | ENSP00000379685.4:n.-39+36415G>A | |
| ENST00000405011.6:c.-193-9239G>A (CYP19A1) | ENSP00000384389.2:n.-193-9239G>A | |
| ENST00000439712.6:c.-282-31640G>A (CYP19A1) | ENSP00000390614.2:n.-282-31640G>A | |
| ENST00000453807.6:c.-229-31693G>A (CYP19A1) | ENSP00000391139.2:n.-229-31693G>A | |
| ENST00000557858.5:c.-38-44451G>A (CYP19A1) | ENSP00000452627.1:n.-38-44451G>A | |
| ENST00000557934.5:c.-38-44451G>A (CYP19A1) | ENSP00000454004.1:n.-38-44451G>A | |
| ENST00000558328.5:c.-38-44451G>A (CYP19A1) | ENSP00000453280.1:n.-38-44451G>A | |
| ENST00000559646.1:c.-39+31032G>A (CYP19A1) | ENSP00000453318.1:n.-39+31032G>A | |
| ENST00000559980.5:c.-282-31640G>A (CYP19A1) | ENSP00000452872.1:n.-282-31640G>A | |
| ENST00000561075.5:c.-38-44451G>A (CYP19A1) | ENSP00000454039.1:n.-38-44451G>A | |
| NM_000103.3:c.-38-44451G>A (CYP19A1) | NP_000094.2:n.-38-44451G>A | |
| NM_031226.2:c.-39+36415G>A (CYP19A1) | NP_112503.1:n.-39+36415G>A | |
| XM_005254191.1:c.-39+31032G>A (CYP19A1) | XP_005254248.1:n.-39+31032G>A | |
| XR_932221.1:n.5385+6094C>T (PIRC66) | ||
| NM_001347248.1:c.-39+36415G>A (CYP19A1) | NP_001334177.1:n.-39+36415G>A | |
| NM_001347249.1:c.-39+31032G>A (CYP19A1) | NP_001334178.1:n.-39+31032G>A | |
| NM_001347250.1:c.-39+849G>A (CYP19A1) | NP_001334179.1:n.-39+849G>A | |
| NR_146310.1:n.263-6213C>T (MIR4713HG) | ||
| NM_000103.4:c.-38-44451G>A (CYP19A1) MANE Select | NP_000094.2:n.-38-44451G>A | |
| NM_001347249.2:c.-39+31032G>A (CYP19A1) | NP_001334178.1:n.-39+31032G>A | |
| NM_031226.3:c.-39+36415G>A (CYP19A1) | NP_112503.1:n.-39+36415G>A | |
| NM_001347250.2:c.-39+849G>A (CYP19A1) | NP_001334179.1:n.-39+849G>A |