Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50185065T>G , CM000679.2:g.50185065T>G | GRCh38 |
| NC_000017.10:g.48262426T>G , CM000679.1:g.48262426T>G | GRCh37 |
| NC_000017.9:g.45617425T>G | NCBI36 |
| NG_007400.1:g.21575A>C , LRG_1:g.21575A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000225964.10:c.*437A>C MANE Select | ENSP00000225964.6:n.*437A>C | |
| ENST00000225964.9:c.*437A>C | ENSP00000225964.5:n.*437A>C | |
| NM_000088.3:c.*437A>C , LRG_1t1:c.*437A>C | NP_000079.2:n.*437A>C | |
| XM_005257058.3:c.*437A>C | XP_005257115.2:n.*437A>C | |
| XM_005257059.3:c.*437A>C | XP_005257116.2:n.*437A>C | |
| XM_011524341.1:c.*437A>C | XP_011522643.1:n.*437A>C | |
| XM_005257058.4:c.*437A>C | XP_005257115.2:n.*437A>C | |
| XM_005257059.4:c.*437A>C | XP_005257116.2:n.*437A>C | |
| NM_000088.4:c.*437A>C MANE Select | NP_000079.2:n.*437A>C |