Linked Data
gnomAD v4:
4-52038269-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52038269C>T , CM000666.2:g.52038269C>T | GRCh38 |
| NC_000004.11:g.52904435C>T , CM000666.1:g.52904435C>T | GRCh37 |
| NC_000004.10:g.52599192C>T | NCBI36 |
| NG_008891.1:g.5051G>A , LRG_204:g.5051G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381431.10:c.-10G>A MANE Select | ENSP00000370839.6:n.-10G>A | |
| ENST00000381431.9:c.-10G>A | ENSP00000370839.5:n.-10G>A | |
| NM_000232.4:c.-10G>A , LRG_204t1:c.-10G>A | NP_000223.1:n.-10G>A | |
| XM_011534403.1:c.-10G>A | XP_011532705.1:n.-10G>A | |
| NM_000232.5:c.-10G>A MANE Select | NP_000223.1:n.-10G>A |