Linked Data
gnomAD v4:
21-31667441-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31667441T>C , CM000683.2:g.31667441T>C | GRCh38 |
| NC_000021.8:g.33039754T>C , CM000683.1:g.33039754T>C | GRCh37 |
| NC_000021.7:g.31961625T>C | NCBI36 |
| NG_008689.1:g.12820T>C , LRG_652:g.12820T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270142.11:c.357+66T>C MANE Select | ENSP00000270142.7:n.357+66T>C | |
| ENST00000270142.10:c.357+66T>C | ENSP00000270142.6:n.357+66T>C | |
| ENST00000389995.4:c.300+66T>C | ENSP00000374645.4:n.300+66T>C | |
| ENST00000470944.1:n.1285+66T>C | ||
| NM_000454.4:c.357+66T>C , LRG_652t1:c.357+66T>C | NP_000445.1:n.357+66T>C | |
| NM_000454.5:c.357+66T>C MANE Select | NP_000445.1:n.357+66T>C |