Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107793752G>T , CM000669.2:g.107793752G>T | GRCh38 |
| NC_000007.13:g.107434197G>T , CM000669.1:g.107434197G>T | GRCh37 |
| NC_000007.12:g.107221433G>T | NCBI36 |
| NG_008046.1:g.14482C>A , LRG_683:g.14482C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000111.3:c.261C>A MANE Select | NP_000102.1:p.Ala87= |
| ENST00000340010.10:c.261C>A MANE Select | ENSP00000345873.5:p.Ala87= |
| NM_000111.2:c.261C>A , LRG_683t1:c.261C>A | NP_000102.1:p.Ala87= |
| ENST00000340010.9:c.261C>A | ENSP00000345873.5:p.Ala87= |
| ENST00000379083.7:c.*52C>A | ENSP00000368375.3:n.*52C>A |
| ENST00000453332.1:c.261C>A | ENSP00000395955.1:p.Ala87= |
| XM_011515867.1:c.261C>A | XP_011514169.1:p.Ala87= |