Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.97697296T= , CM000671.2:g.97697296T= | GRCh38 |
| NC_000009.11:g.100459578T= , CM000671.1:g.100459578T= | GRCh37 |
| NC_000009.10:g.99499399T= | NCBI36 |
| NG_011642.1:g.5114A= , LRG_471:g.5114A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000380.4:c.-4A= MANE Select | NP_000371.1:n.-4A= |
| ENST00000375128.5:c.-4A= MANE Select | ENSP00000364270.5:n.-4A= |
| NM_000380.3:c.-4A= , LRG_471t1:c.-4A= | NP_000371.1:n.-4A= |
| NM_001354975.1:c.-1153A= | NP_001341904.1:n.-1153A= |
| NM_001354975.2:c.-1153A= | NP_001341904.1:n.-1153A= |
| NR_027302.1:n.114A= | |
| NR_027302.2:n.45A= | |
| NR_149091.1:n.114A= | |
| NR_149091.2:n.45A= | |
| NR_149092.1:n.114A= | |
| NR_149092.2:n.45A= | |
| NR_149093.1:n.114A= | |
| NR_149093.2:n.45A= | |
| NR_149094.1:n.114A= | |
| NR_149094.2:n.45A= | |
| ENST00000375128.4:c.-4A= | ENSP00000364270.4:n.-4A= |
| XM_006717278.1:c.-4A= | XP_006717341.1:n.-4A= |
| XM_011518988.1:c.-4A= | XP_011517290.1:n.-4A= |
| XR_929839.1:n.108A= |