Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110601876C= , CM000672.2:g.110601876C= | GRCh38 |
| NC_000010.10:g.112361634C= , CM000672.1:g.112361634C= | GRCh37 |
| NC_000010.9:g.112351624C= | NCBI36 |
| NG_012217.1:g.39186C= , LRG_774:g.39186C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005445.4:c.2884C= MANE Select | NP_005436.1:p.Leu962= |
| ENST00000361804.5:c.2884C= MANE Select | ENSP00000354720.5:p.Leu962= |
| NM_005445.3:c.2884C= , LRG_774t1:c.2884C= | NP_005436.1:p.Leu962= |
| ENST00000361804.4:c.2884C= | ENSP00000354720.4:p.Leu962= |
| ENST00000684988.1:n.5117C= | |
| ENST00000685743.1:n.2592C= | |
| ENST00000686057.1:n.1235C= | |
| ENST00000689321.1:n.1847C= | |
| ENST00000689986.1:n.673C= |