Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.49451664T>C , CM000668.2:g.49451664T>C | GRCh38 |
| NC_000006.11:g.49419377T>C , CM000668.1:g.49419377T>C | GRCh37 |
| NC_000006.10:g.49527336T>C | NCBI36 |
| NG_007100.1:g.16476A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274813.4:c.1134A>G MANE Select | ENSP00000274813.3:p.Val378= | |
| ENST00000274813.3:c.1134A>G | ENSP00000274813.3:p.Val378= | |
| NM_000255.3:c.1134A>G | NP_000246.2:p.Val378= | |
| XM_005249143.2:c.1134A>G | XP_005249200.1:p.Val378= | |
| XM_005249143.3:c.1134A>G | XP_005249200.1:p.Val378= | |
| NM_000255.4:c.1134A>G MANE Select | NP_000246.2:p.Val378= |