Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.44305705A>G , CM000667.2:g.44305705A>G | GRCh38 |
| NC_000005.9:g.44305807A>G , CM000667.1:g.44305807A>G | GRCh37 |
| NC_000005.8:g.44341564A>G | NCBI36 |
| NG_011446.1:g.87978T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264664.5:c.430-513T>C MANE Select | ENSP00000264664.4:n.430-513T>C | |
| ENST00000264664.4:c.430-513T>C | ENSP00000264664.4:n.430-513T>C | |
| NM_004465.1:c.430-513T>C | NP_004456.1:n.430-513T>C | |
| XM_005248264.2:c.430-513T>C | XP_005248321.1:n.430-513T>C | |
| XM_005248264.4:c.430-513T>C | XP_005248321.1:n.430-513T>C | |
| NM_004465.2:c.430-513T>C MANE Select | NP_004456.1:n.430-513T>C |