Linked Data
gnomAD v4:
20-35176757-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.35176757A>G , CM000682.2:g.35176757A>G | GRCh38 |
| NC_000020.10:g.33764560A>G , CM000682.1:g.33764560A>G | GRCh37 |
| NC_000020.9:g.33228221A>G | NCBI36 |
| NG_032899.1:g.9787A>G | |
| NG_032899.2:g.9787A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000216968.5:c.661A>G MANE Select | ENSP00000216968.3:p.Ile221Val | |
| ENST00000216968.4:c.661A>G | ENSP00000216968.3:p.Ile221Val | |
| ENST00000634509.1:c.94+311A>G | ENSP00000489456.1:n.94+311A>G | |
| ENST00000635377.1:c.501+311A>G | ||
| NM_006404.4:c.661A>G | NP_006395.2:p.Ile221Val | |
| XM_011528496.1:c.601+311A>G | XP_011526798.1:n.601+311A>G | |
| NM_001355008.1:c.-101-10886T>C | NP_001341937.1:n.-101-10886T>C | |
| NM_006404.5:c.661A>G MANE Select | NP_006395.2:p.Ile221Val | |
| NM_001355008.2:c.-101-10886T>C | NP_001341937.1:n.-101-10886T>C |