Linked Data
gnomAD v4:
2-48755736-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.48755736C>A , CM000664.2:g.48755736C>A | GRCh38 |
| NC_000002.11:g.48982875C>A , CM000664.1:g.48982875C>A | GRCh37 |
| NC_000002.10:g.48836379C>A | NCBI36 |
| NG_008193.1:g.5006G>T | |
| NG_033050.1:g.230812C>A | |
| NG_008193.2:g.5006G>T | |
| NG_033050.2:g.230812C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000402114.6:c.3442-20544C>A (STON1-GTF2A1L) | ENSP00000385701.1:n.3442-20544C>A | |
| NM_000233.3:c.-65G>T (LHCGR) | NP_000224.2:n.-65G>T | |
| NM_001198593.1:c.3442-20544C>A (STON1-GTF2A1L) | NP_001185522.1:n.3442-20544C>A | |
| NM_001198593.2:c.3442-20544C>A (STON1-GTF2A1L) | NP_001185522.1:n.3442-20544C>A |