Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154837586A>G , CM000685.2:g.154837586A>G | GRCh38 |
| NC_000023.10:g.154065861A>G , CM000685.1:g.154065861A>G | GRCh37 |
| NC_000023.9:g.153719055A>G | NCBI36 |
| NG_011403.1:g.190138T>C | |
| NG_033065.1:g.2077T>C | |
| NG_011403.2:g.190138T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000132.4:c.*11T>C MANE Select | NP_000123.1:n.*11T>C |
| ENST00000360256.9:c.*11T>C MANE Select | ENSP00000353393.4:n.*11T>C |
| NM_000132.3:c.*11T>C | NP_000123.1:n.*11T>C |
| NM_019863.2:c.*11T>C | NP_063916.1:n.*11T>C |
| NM_019863.3:c.*11T>C | NP_063916.1:n.*11T>C |
| ENST00000330287.10:c.*11T>C | ENSP00000327895.6:n.*11T>C |
| ENST00000360256.8:c.*11T>C | ENSP00000353393.4:n.*11T>C |
| ENST00000644698.1:c.*11T>C | ENSP00000495706.1:n.*11T>C |
| XM_011531126.1:c.*11T>C | XP_011529428.1:n.*11T>C |