Linked Data
ClinVar Variation Id:
924538
dbSNP Id:
rs1478242707
gnomAD v2:
6-7585883-T-C
gnomAD v4:
6-7585650-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.7585650T>C , CM000668.2:g.7585650T>C | GRCh38 |
| NC_000006.11:g.7585883T>C , CM000668.1:g.7585883T>C | GRCh37 |
| NC_000006.10:g.7530882T>C | NCBI36 |
| NG_008803.1:g.49014T>C , LRG_423:g.49014T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710359.1:c.7059T>C | ENSP00000518230.1:p.Asp2353= | |
| ENST00000379802.8:c.8388T>C MANE Select | ENSP00000369129.3:p.Asp2796= | |
| ENST00000379802.7:c.8388T>C | ENSP00000369129.3:p.Asp2796= | |
| ENST00000418664.2:c.6591T>C | ENSP00000396591.2:p.Asp2197= | |
| NM_001008844.1:c.6591T>C | NP_001008844.1:p.Asp2197= | |
| NM_004415.2:c.8388T>C , LRG_423t1:c.8388T>C | NP_004406.2:p.Asp2796= | |
| XM_011514323.1:c.7059T>C | XP_011512625.1:p.Asp2353= | |
| NM_001008844.2:c.6591T>C | NP_001008844.1:p.Asp2197= | |
| NM_001319034.1:c.7059T>C | NP_001305963.1:p.Asp2353= | |
| NM_004415.3:c.8388T>C | NP_004406.2:p.Asp2796= | |
| NM_004415.4:c.8388T>C MANE Select | NP_004406.2:p.Asp2796= | |
| NM_001008844.3:c.6591T>C | NP_001008844.1:p.Asp2197= | |
| NM_001319034.2:c.7059T>C | NP_001305963.1:p.Asp2353= |