Linked Data
gnomAD v4:
1-94002129-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94002129C>A , CM000663.2:g.94002129C>A | GRCh38 |
| NC_000001.10:g.94467685C>A , CM000663.1:g.94467685C>A | GRCh37 |
| NC_000001.9:g.94240273C>A | NCBI36 |
| NG_009073.1:g.124021G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.6148-137G>T MANE Select | ENSP00000359245.3:n.6148-137G>T | |
| ENST00000370225.3:c.6148-137G>T | ENSP00000359245.3:n.6148-137G>T | |
| ENST00000465352.1:n.564-137G>T | ||
| ENST00000536513.5:c.2524-137G>T | ENSP00000439707.2:n.2524-137G>T | |
| NM_000350.2:c.6148-137G>T | NP_000341.2:n.6148-137G>T | |
| NM_000350.3:c.6148-137G>T MANE Select | NP_000341.2:n.6148-137G>T |