Linked Data
ClinVar Variation Id:
360293
dbSNP Id:
rs2908275
gnomAD v2:
7-44184258-G-A
gnomAD v3:
7-44144659-G-A
gnomAD v4:
7-44144659-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.44144659G>A , CM000669.2:g.44144659G>A | GRCh38 |
| NC_000007.13:g.44184258G>A , CM000669.1:g.44184258G>A | GRCh37 |
| NC_000007.12:g.44150783G>A | NCBI36 |
| NG_008847.1:g.49765C>T | |
| NG_008847.2:g.58512C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395796.8:c.*1873C>T | ENSP00000379142.4:n.*1873C>T | |
| ENST00000616242.5:c.*995C>T | ENSP00000482149.2:n.*995C>T | |
| ENST00000683378.1:n.1101C>T | ||
| ENST00000336642.9:c.*477C>T | ENSP00000338009.5:n.*477C>T | |
| ENST00000345378.7:c.*477C>T | ENSP00000223366.2:n.*477C>T | |
| ENST00000403799.8:c.*477C>T MANE Select | ENSP00000384247.3:n.*477C>T | |
| ENST00000671824.1:c.*477C>T | ENSP00000500264.1:n.*477C>T | |
| ENST00000672743.1:n.382-423C>T | ||
| ENST00000673284.1:c.1370-423C>T | ENSP00000499852.1:n.1370-423C>T | |
| ENST00000336642.8:c.927C>T | ENSP00000338009.4:n.927C>T | |
| ENST00000345378.6:c.*477C>T | ENSP00000223366.2:n.*477C>T | |
| ENST00000395796.7:c.*477C>T | ENSP00000379142.3:n.*477C>T | |
| ENST00000403799.7:c.*477C>T | ENSP00000384247.3:n.*477C>T | |
| ENST00000459642.1:n.1255C>T | ||
| ENST00000616242.4:c.1872C>T | ENSP00000482149.1:n.1872C>T | |
| NM_000162.3:c.*477C>T | NP_000153.1:n.*477C>T | |
| NM_033507.1:c.*477C>T | NP_277042.1:n.*477C>T | |
| NM_033508.1:c.*477C>T | NP_277043.1:n.*477C>T | |
| NM_000162.4:c.*477C>T | NP_000153.1:n.*477C>T | |
| NM_001354800.1:c.1370-423C>T | NP_001341729.1:n.1370-423C>T | |
| NM_001354801.1:c.*477C>T | NP_001341730.1:n.*477C>T | |
| NM_001354802.1:c.230-423C>T | NP_001341731.1:n.230-423C>T | |
| NM_001354803.1:c.*477C>T | NP_001341732.1:n.*477C>T | |
| NM_033507.2:c.*477C>T | NP_277042.1:n.*477C>T | |
| NM_033508.2:c.*477C>T | NP_277043.1:n.*477C>T | |
| XM_024446707.1:c.*477C>T | XP_024302475.1:n.*477C>T | |
| NM_000162.5:c.*477C>T MANE Select | NP_000153.1:n.*477C>T | |
| NM_033507.3:c.*477C>T | NP_277042.1:n.*477C>T | |
| NM_033508.3:c.*477C>T | NP_277043.1:n.*477C>T | |
| NM_001354803.2:c.*477C>T | NP_001341732.1:n.*477C>T |