Linked Data
gnomAD v4:
8-86670980-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86670980C>T , CM000670.2:g.86670980C>T | GRCh38 |
| NC_000008.10:g.87683208C>T , CM000670.1:g.87683208C>T | GRCh37 |
| NC_000008.9:g.87752324C>T | NCBI36 |
| NG_016980.1:g.77696G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.457G>A MANE Select | ENSP00000316605.5:p.Gly153Arg | |
| ENST00000680314.1:n.218G>A | ||
| ENST00000681746.1:c.457G>A | ENSP00000505959.1:p.Gly153Arg | |
| ENST00000320005.5:c.457G>A | ENSP00000316605.5:p.Gly153Arg | |
| NM_019098.4:c.457G>A | NP_061971.3:p.Gly153Arg | |
| XM_011517138.1:c.43G>A | XP_011515440.1:p.Gly15Arg | |
| XM_011517138.2:c.43G>A | XP_011515440.1:p.Gly15Arg | |
| NM_019098.5:c.457G>A MANE Select | NP_061971.3:p.Gly153Arg |