Linked Data
ClinVar Variation Id:
532706
ClinVar RCV Id:
RCV002440271
dbSNP Id:
rs149518815
ExAC:
16:11650560 C / T
gnomAD v2:
16-11650560-C-T
gnomAD v3:
16-11556704-C-T
gnomAD v4:
16-11556704-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.11556704C>T , CM000678.2:g.11556704C>T | GRCh38 |
| NC_000016.9:g.11650560C>T , CM000678.1:g.11650560C>T | GRCh37 |
| NC_000016.8:g.11558061C>T | NCBI36 |
| NG_009008.1:g.35247G>A , LRG_253:g.35247G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000622633.5:c.27G>A MANE Select | ENSP00000483114.1:p.Ala9= | |
| ENST00000339430.9:c.27G>A | ENSP00000340118.5:p.Ala9= | |
| ENST00000381810.7:c.27G>A | ENSP00000371231.3:p.Ala9= | |
| ENST00000413364.6:c.27G>A | ENSP00000397958.2:p.Ala9= | |
| ENST00000570798.5:c.27G>A | ENSP00000458871.1:p.Ala9= | |
| ENST00000570904.5:c.27G>A | ENSP00000459138.1:p.Ala9= | |
| ENST00000571277.1:c.27G>A | ENSP00000459026.1:p.Ala9= | |
| ENST00000571459.5:c.27G>A | ENSP00000459603.1:p.Ala9= | |
| ENST00000571627.5:c.27G>A | ENSP00000460743.1:p.Ala9= | |
| ENST00000571688.5:c.27G>A | ENSP00000459533.1:p.Ala9= | |
| ENST00000571976.1:c.27G>A | ENSP00000460133.1:p.Ala9= | |
| ENST00000572255.5:c.-59-3015G>A | ENSP00000458836.1:n.-59-3015G>A | |
| ENST00000573332.5:c.27G>A | ENSP00000460873.1:p.Ala9= | |
| ENST00000574701.5:c.27G>A | ENSP00000458981.1:p.Ala9= | |
| ENST00000574703.5:c.27G>A | ENSP00000459913.1:p.Ala9= | |
| ENST00000574763.5:c.27G>A | ENSP00000461813.1:p.Ala9= | |
| ENST00000574848.5:c.117G>A | ENSP00000459898.1:p.Ala39= | |
| ENST00000576036.5:c.27G>A | ENSP00000461667.1:p.Ala9= | |
| ENST00000620789.4:c.27G>A | ENSP00000481589.1:p.Ala9= | |
| ENST00000622633.4:c.27G>A | ENSP00000483114.1:p.Ala9= | |
| NM_001136472.1:c.27G>A | NP_001129944.1:p.Ala9= | |
| NM_001136473.1:c.27G>A , LRG_253t1:c.27G>A | NP_001129945.1:p.Ala9= | |
| NM_004862.3:c.27G>A | NP_004853.2:p.Ala9= | |
| NR_024320.1:n.161G>A | ||
| XM_006720982.2:c.27G>A | XP_006721045.1:p.Ala9= | |
| XM_006720983.2:c.27G>A | XP_006721046.1:p.Ala9= | |
| XM_006720984.2:c.27G>A | XP_006721047.1:p.Ala9= | |
| XM_006720985.2:c.27G>A | XP_006721048.1:p.Ala9= | |
| XM_011522754.1:c.117G>A | XP_011521056.1:p.Ala39= | |
| XM_006720982.3:c.27G>A | XP_006721045.1:p.Ala9= | |
| XM_006720983.4:c.27G>A | XP_006721046.1:p.Ala9= | |
| XM_006720984.4:c.27G>A | XP_006721047.1:p.Ala9= | |
| XM_006720985.3:c.27G>A | XP_006721048.1:p.Ala9= | |
| XM_011522754.3:c.117G>A | XP_011521056.1:p.Ala39= | |
| XM_017023896.1:c.27G>A | XP_016879385.1:p.Ala9= | |
| NM_001136472.2:c.27G>A MANE Select | NP_001129944.1:p.Ala9= | |
| NM_004862.4:c.27G>A | NP_004853.2:p.Ala9= | |
| NR_024320.2:n.161G>A |