Linked Data
gnomAD v4:
9-98542022-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.98542022G>C , CM000671.2:g.98542022G>C | GRCh38 |
| NC_000009.11:g.101304304G>C , CM000671.1:g.101304304G>C | GRCh37 |
| NC_000009.10:g.100344125G>C | NCBI36 |
| NG_016426.1:g.172176C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259455.4:c.481C>G MANE Select | ENSP00000259455.2:p.Pro161Ala | |
| ENST00000637410.1:n.259C>G | ||
| ENST00000637717.1:c.97C>G | ENSP00000490789.1:p.Pro33Ala | |
| ENST00000638001.1:n.91C>G | ||
| ENST00000259455.3:c.481C>G | ENSP00000259455.2:p.Pro161Ala | |
| ENST00000477471.1:n.268C>G | ||
| ENST00000634227.1:n.255C>G | ||
| NM_005458.7:c.481C>G | NP_005449.5:p.Pro161Ala | |
| XM_017015331.2:c.187C>G | XP_016870820.1:p.Pro63Ala | |
| NM_005458.8:c.481C>G MANE Select | NP_005449.5:p.Pro161Ala |