Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.163324721T>A , CM000666.2:g.163324721T>A | GRCh38 |
| NC_000004.11:g.164245873T>A , CM000666.1:g.164245873T>A | GRCh37 |
| NC_000004.10:g.164465323T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000296533.3:c.*582A>T MANE Select | ENSP00000354652.2:n.*582A>T | |
| ENST00000296533.2:c.*582A>T | ENSP00000354652.2:n.*582A>T | |
| NM_000909.5:c.*582A>T | NP_000900.1:n.*582A>T | |
| XM_005263031.2:c.*582A>T | XP_005263088.1:n.*582A>T | |
| XM_011532010.1:c.*582A>T | XP_011530312.1:n.*582A>T | |
| XM_005263031.4:c.*582A>T | XP_005263088.1:n.*582A>T | |
| XM_011532010.3:c.*582A>T | XP_011530312.1:n.*582A>T | |
| NM_000909.6:c.*582A>T MANE Select | NP_000900.1:n.*582A>T |