Linked Data
gnomAD v4:
4-99949525-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99949525T>G , CM000666.2:g.99949525T>G | GRCh38 |
| NC_000004.11:g.100870682T>G , CM000666.1:g.100870682T>G | GRCh37 |
| NC_000004.10:g.101089705T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296417.6:c.82-139A>C MANE Select | ENSP00000296417.5:n.82-139A>C | |
| ENST00000651623.1:c.82-139A>C | ENSP00000498935.1:n.82-139A>C | |
| ENST00000296417.5:c.82-139A>C | ENSP00000296417.5:n.82-139A>C | |
| ENST00000511203.1:n.775A>C | ||
| ENST00000511319.5:n.607-139A>C | ||
| ENST00000511348.1:n.404A>C | ||
| ENST00000527366.1:n.165+138A>C | ||
| ENST00000529158.5:n.131-139A>C | ||
| NM_002106.3:c.82-139A>C | NP_002097.1:n.82-139A>C | |
| NM_002106.4:c.82-139A>C MANE Select | NP_002097.1:n.82-139A>C |