Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.33438899A>G , CM000682.2:g.33438899A>G | GRCh38 |
| NC_000020.10:g.32026705A>G , CM000682.1:g.32026705A>G | GRCh37 |
| NC_000020.9:g.31490366A>G | NCBI36 |
| NG_011622.1:g.9994T>C , LRG_332:g.9994T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217381.3:c.438T>C MANE Select | ENSP00000217381.2:p.Ala146= | |
| ENST00000217381.2:c.438T>C | ENSP00000217381.2:p.Ala146= | |
| NM_003098.2:c.438T>C , LRG_332t1:c.438T>C | NP_003089.1:p.Ala146= | |
| XM_005260517.1:c.438T>C | XP_005260574.1:p.Ala146= | |
| XM_011529007.1:c.438T>C | XP_011527309.1:p.Ala146= | |
| XM_011529008.1:c.438T>C | XP_011527310.1:p.Ala146= | |
| XR_936612.1:n.671T>C | ||
| XM_024451971.1:c.111T>C | XP_024307739.1:p.Ala37= | |
| NM_003098.3:c.438T>C MANE Select | NP_003089.1:p.Ala146= |