Linked Data
gnomAD v4:
8-86632873-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86632873C>G , CM000670.2:g.86632873C>G | GRCh38 |
| NC_000008.10:g.87645101C>G , CM000670.1:g.87645101C>G | GRCh37 |
| NC_000008.9:g.87714217C>G | NCBI36 |
| NG_016980.1:g.115803G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320005.6:c.1199G>C MANE Select | ENSP00000316605.5:p.Trp400Ser | |
| ENST00000681546.1:n.1019G>C | ||
| ENST00000681746.1:c.1199G>C | ENSP00000505959.1:p.Trp400Ser | |
| ENST00000320005.5:c.1199G>C | ENSP00000316605.5:p.Trp400Ser | |
| NM_019098.4:c.1199G>C | NP_061971.3:p.Trp400Ser | |
| XM_011517138.1:c.785G>C | XP_011515440.1:p.Trp262Ser | |
| XM_011517138.2:c.785G>C | XP_011515440.1:p.Trp262Ser | |
| NM_019098.5:c.1199G>C MANE Select | NP_061971.3:p.Trp400Ser |