Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.108378337A= , CM000664.2:g.108378337A= | GRCh38 |
| NC_000002.11:g.108994793A= , CM000664.1:g.108994793A= | GRCh37 |
| NC_000002.10:g.108361225A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272452.7:c.-1A= MANE Select | ENSP00000272452.2:n.-1A= | |
| ENST00000272452.6:c.-1A= | ENSP00000272452.2:n.-1A= | |
| ENST00000409309.3:c.-1A= | ENSP00000387225.3:n.-1A= | |
| ENST00000494122.1:n.427A= | ||
| NM_006588.2:c.-1A= | NP_006579.2:n.-1A= | |
| XM_005263919.2:c.-1A= | XP_005263976.1:n.-1A= | |
| NM_001321770.1:c.-1A= | NP_001308699.1:n.-1A= | |
| NM_006588.3:c.-1A= | NP_006579.2:n.-1A= | |
| NR_135776.1:n.427A= | ||
| NR_135779.1:n.427A= | ||
| NM_006588.4:c.-1A= MANE Select | NP_006579.2:n.-1A= | |
| NM_001321770.2:c.-1A= | NP_001308699.1:n.-1A= | |
| NR_135776.2:n.384A= | ||
| NR_135779.2:n.384A= |