Linked Data
gnomAD v4:
16-2317785-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2317785G>T , CM000678.2:g.2317785G>T | GRCh38 |
| NC_000016.9:g.2367786G>T , CM000678.1:g.2367786G>T | GRCh37 |
| NC_000016.8:g.2307787G>T | NCBI36 |
| NG_011790.1:g.27962C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301732.10:c.874-21C>A MANE Select | ENSP00000301732.5:n.874-21C>A | |
| ENST00000301732.9:c.874-21C>A | ENSP00000301732.5:n.874-21C>A | |
| ENST00000382381.7:c.874-21C>A | ENSP00000371818.3:n.874-21C>A | |
| ENST00000563623.5:n.1437-21C>A | ||
| NM_001089.2:c.874-21C>A | NP_001080.2:n.874-21C>A | |
| NM_001089.3:c.874-21C>A MANE Select | NP_001080.2:n.874-21C>A |