Linked Data
dbSNP Id:
rs2038883237
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.74917541G>C , CM000679.2:g.74917541G>C | GRCh38 |
| NC_000017.10:g.72913635G>C , CM000679.1:g.72913635G>C | GRCh37 |
| NC_000017.9:g.70425230G>C | NCBI36 |
| NG_007882.1:g.10717C>G | |
| NG_007882.2:g.10723C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614341.5:c.*532C>G MANE Select | ENSP00000480279.1:n.*532C>G | |
| ENST00000614341.4:c.*532C>G | ENSP00000480279.1:n.*532C>G | |
| NM_001282489.2:c.*532C>G | NP_001269418.1:n.*532C>G | |
| NM_173477.4:c.*532C>G | NP_775748.2:n.*532C>G | |
| XM_011524296.1:c.*532C>G | XP_011522598.1:n.*532C>G | |
| XM_011524296.2:c.*532C>G | XP_011522598.1:n.*532C>G | |
| NM_173477.5:c.*532C>G MANE Select | NP_775748.2:n.*532C>G | |
| NM_001282489.3:c.*532C>G | NP_001269418.1:n.*532C>G |