MyVariant.info:
GRCh38
chr15:g.74723851G>C
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74723851G>C , CM000677.2:g.74723851G>C | GRCh38 |
| NC_000015.9:g.75016192G>C , CM000677.1:g.75016192G>C | GRCh37 |
| NC_000015.8:g.72803245G>C | NCBI36 |
| NG_008431.1:g.6310G>C | |
| NG_008431.2:g.6310G>C | |
| NG_061374.1:g.6678C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379727.8:c.-29-725C>G MANE Select | ENSP00000369050.3:n.-29-725C>G | |
| ENST00000379727.7:c.-29-725C>G | ENSP00000369050.3:n.-29-725C>G | |
| ENST00000395048.6:c.-26-728C>G | ENSP00000378488.2:n.-26-728C>G | |
| ENST00000395049.8:c.-29-725C>G | ENSP00000378489.4:n.-29-725C>G | |
| ENST00000562201.5:c.-26-728C>G | ENSP00000455340.1:n.-26-728C>G | |
| ENST00000564596.5:c.-220-1317C>G | ENSP00000457668.1:n.-220-1317C>G | |
| ENST00000566503.1:c.-220-1317C>G | ENSP00000455846.1:n.-220-1317C>G | |
| ENST00000567032.5:c.-29-725C>G | ENSP00000456585.1:n.-29-725C>G | |
| ENST00000569630.5:c.-26-728C>G | ENSP00000455051.1:n.-26-728C>G | |
| ENST00000617691.4:c.-26-728C>G | ENSP00000482863.1:n.-26-728C>G | |
| NM_000499.3:c.-26-728C>G | NP_000490.1:n.-26-728C>G | |
| XM_005254185.1:c.-29-725C>G | XP_005254242.1:n.-29-725C>G | |
| NM_000499.5:c.-26-728C>G | NP_000490.1:n.-26-728C>G | |
| NM_001319216.2:c.-29-725C>G | NP_001306145.1:n.-29-725C>G | |
| NM_001319217.2:c.-29-725C>G MANE Select | NP_001306146.1:n.-29-725C>G |