Linked Data
gnomAD v4:
5-174724598-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.174724598A>T , CM000667.2:g.174724598A>T | GRCh38 |
| NC_000005.9:g.174151601A>T , CM000667.1:g.174151601A>T | GRCh37 |
| NC_000005.8:g.174084207A>T | NCBI36 |
| NG_008124.1:g.5027A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239243.7:c.-62A>T MANE Select | ENSP00000239243.5:n.-62A>T | |
| ENST00000239243.6:c.-62A>T | ENSP00000239243.5:n.-62A>T | |
| NM_002449.4:c.-62A>T | NP_002440.2:n.-62A>T | |
| NM_001363626.1:c.-62A>T | NP_001350555.1:n.-62A>T | |
| NM_002449.5:c.-62A>T MANE Select | NP_002440.2:n.-62A>T | |
| NM_001363626.2:c.-62A>T | NP_001350555.1:n.-62A>T |