Linked Data
gnomAD v4:
22-32474859-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32474859T>C , CM000684.2:g.32474859T>C | GRCh38 |
| NC_000022.10:g.32870846T>C , CM000684.1:g.32870846T>C | GRCh37 |
| NC_000022.9:g.31200846T>C | NCBI36 |
| NG_016001.1:g.5140T>C | |
| NG_016001.2:g.5140T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266087.12:c.-144T>C MANE Select | ENSP00000266087.7:n.-144T>C | |
| ENST00000266087.11:c.-144T>C | ENSP00000266087.7:n.-144T>C | |
| ENST00000420700.5:c.-144T>C | ENSP00000406155.1:n.-144T>C | |
| ENST00000425028.5:c.-144T>C | ENSP00000395823.1:n.-144T>C | |
| NM_012179.3:c.-144T>C | NP_036311.3:n.-144T>C | |
| XM_011530106.1:c.-317T>C | XP_011528408.1:n.-317T>C | |
| XM_024452207.1:c.-334T>C | XP_024307975.1:n.-334T>C | |
| NM_012179.4:c.-144T>C MANE Select | NP_036311.3:n.-144T>C |