Linked Data
gnomAD v4:
17-29451513-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.29451513T>C , CM000679.2:g.29451513T>C | GRCh38 |
| NC_000017.10:g.27778531T>C , CM000679.1:g.27778531T>C | GRCh37 |
| NC_000017.9:g.24802657T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261716.8:c.-36T>C MANE Select | ENSP00000261716.3:n.-36T>C | |
| ENST00000261716.7:c.-36T>C | ENSP00000261716.3:n.-36T>C | |
| ENST00000536202.1:c.-36T>C | ENSP00000438819.1:n.-36T>C | |
| ENST00000583121.5:c.-36T>C | ENSP00000464562.1:n.-36T>C | |
| ENST00000587277.1:n.159T>C | ||
| NM_020791.2:c.-36T>C | NP_065842.1:n.-36T>C | |
| NM_025142.1:c.-36T>C | NP_079418.1:n.-36T>C | |
| XM_011525060.1:c.-36T>C | XP_011523362.1:n.-36T>C | |
| XM_011525060.2:c.-36T>C | XP_011523362.1:n.-36T>C | |
| NM_020791.4:c.-36T>C MANE Select | NP_065842.1:n.-36T>C |