Linked Data
ClinVar Variation Id:
215840
dbSNP Id:
rs141862602
ExAC:
16:11650441 G / A
gnomAD v2:
16-11650441-G-A
gnomAD v3:
16-11556585-G-A
gnomAD v4:
16-11556585-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.11556585G>A , CM000678.2:g.11556585G>A | GRCh38 |
| NC_000016.9:g.11650441G>A , CM000678.1:g.11650441G>A | GRCh37 |
| NC_000016.8:g.11557942G>A | NCBI36 |
| NG_009008.1:g.35366C>T , LRG_253:g.35366C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622633.5:c.146C>T MANE Select | ENSP00000483114.1:p.Thr49Met | |
| ENST00000339430.9:c.146C>T | ENSP00000340118.5:p.Thr49Met | |
| ENST00000381810.7:c.146C>T | ENSP00000371231.3:p.Thr49Met | |
| ENST00000413364.6:c.146C>T | ENSP00000397958.2:p.Thr49Met | |
| ENST00000570798.5:c.146C>T | ENSP00000458871.1:p.Thr49Met | |
| ENST00000570904.5:c.146C>T | ENSP00000459138.1:p.Thr49Met | |
| ENST00000571459.5:c.146C>T | ENSP00000459603.1:p.Thr49Met | |
| ENST00000571627.5:c.146C>T | ENSP00000460743.1:p.Thr49Met | |
| ENST00000571688.5:c.146C>T | ENSP00000459533.1:p.Thr49Met | |
| ENST00000571976.1:c.146C>T | ENSP00000460133.1:p.Thr49Met | |
| ENST00000572255.5:c.-59-2896C>T | ENSP00000458836.1:n.-59-2896C>T | |
| ENST00000573332.5:c.146C>T | ENSP00000460873.1:p.Thr49Met | |
| ENST00000574701.5:c.146C>T | ENSP00000458981.1:p.Thr49Met | |
| ENST00000574703.5:c.146C>T | ENSP00000459913.1:p.Thr49Met | |
| ENST00000574763.5:c.146C>T | ENSP00000461813.1:p.Thr49Met | |
| ENST00000574848.5:c.236C>T | ENSP00000459898.1:p.Thr79Met | |
| ENST00000576036.5:c.146C>T | ENSP00000461667.1:p.Thr49Met | |
| ENST00000620789.4:c.146C>T | ENSP00000481589.1:p.Thr49Met | |
| ENST00000622633.4:c.146C>T | ENSP00000483114.1:p.Thr49Met | |
| NM_001136472.1:c.146C>T | NP_001129944.1:p.Thr49Met | |
| NM_001136473.1:c.146C>T , LRG_253t1:c.146C>T | NP_001129945.1:p.Thr49Met | |
| NM_004862.3:c.146C>T | NP_004853.2:p.Thr49Met | |
| NR_024320.1:n.280C>T | ||
| XM_006720982.2:c.146C>T | XP_006721045.1:p.Thr49Met | |
| XM_006720983.2:c.146C>T | XP_006721046.1:p.Thr49Met | |
| XM_006720984.2:c.146C>T | XP_006721047.1:p.Thr49Met | |
| XM_006720985.2:c.146C>T | XP_006721048.1:p.Thr49Met | |
| XM_011522754.1:c.236C>T | XP_011521056.1:p.Thr79Met | |
| XM_006720982.3:c.146C>T | XP_006721045.1:p.Thr49Met | |
| XM_006720983.4:c.146C>T | XP_006721046.1:p.Thr49Met | |
| XM_006720984.4:c.146C>T | XP_006721047.1:p.Thr49Met | |
| XM_006720985.3:c.146C>T | XP_006721048.1:p.Thr49Met | |
| XM_011522754.3:c.236C>T | XP_011521056.1:p.Thr79Met | |
| XM_017023896.1:c.146C>T | XP_016879385.1:p.Thr49Met | |
| NM_001136472.2:c.146C>T MANE Select | NP_001129944.1:p.Thr49Met | |
| NM_004862.4:c.146C>T | NP_004853.2:p.Thr49Met | |
| NR_024320.2:n.280C>T |