Linked Data
dbSNP Id:
rs770786127
gnomAD v4:
8-86632865-G-T
MyVariant Identifiers:
chr8:g.87645093G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86632865G>T , CM000670.2:g.86632865G>T | GRCh38 |
| NC_000008.10:g.87645093G>T , CM000670.1:g.87645093G>T | GRCh37 |
| NC_000008.9:g.87714209G>T | NCBI36 |
| NG_016980.1:g.115811C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320005.6:c.1207C>A MANE Select | ENSP00000316605.5:p.Arg403= | |
| ENST00000681546.1:n.1027C>A | ||
| ENST00000681746.1:c.1207C>A | ENSP00000505959.1:p.Arg403= | |
| ENST00000320005.5:c.1207C>A | ENSP00000316605.5:p.Arg403= | |
| NM_019098.4:c.1207C>A | NP_061971.3:p.Arg403= | |
| XM_011517138.1:c.793C>A | XP_011515440.1:p.Arg265= | |
| XM_011517138.2:c.793C>A | XP_011515440.1:p.Arg265= | |
| NM_019098.5:c.1207C>A MANE Select | NP_061971.3:p.Arg403= |