Linked Data
ClinVar Variation Id:
542830
dbSNP Id:
rs866479368
gnomAD v2:
19-13441076-C-T
gnomAD v3:
19-13330262-C-T
gnomAD v4:
19-13330262-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.13330262C>T , CM000681.2:g.13330262C>T | GRCh38 |
| NC_000019.9:g.13441076C>T , CM000681.1:g.13441076C>T | GRCh37 |
| NC_000019.8:g.13302076C>T | NCBI36 |
| NG_011569.1:g.181199G>A , LRG_7:g.181199G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360228.11:c.1327G>A MANE Select | ENSP00000353362.5:p.Ala443Thr | |
| ENST00000573710.7:c.1333G>A | ENSP00000460092.3:p.Ala445Thr | |
| ENST00000635727.1:c.1330G>A | ENSP00000490001.1:p.Ala444Thr | |
| ENST00000635895.1:c.1330G>A | ENSP00000490323.1:p.Ala444Thr | |
| ENST00000636012.1:c.1330G>A | ENSP00000490223.1:p.Ala444Thr | |
| ENST00000636022.1:n.194G>A | ||
| ENST00000636389.1:c.1330G>A | ENSP00000489992.1:p.Ala444Thr | |
| ENST00000636549.1:c.1330G>A | ENSP00000490578.1:p.Ala444Thr | |
| ENST00000636974.1:n.689G>A | ||
| ENST00000637276.1:c.1330G>A | ENSP00000489777.1:p.Ala444Thr | |
| ENST00000637432.1:c.1330G>A | ENSP00000490617.1:p.Ala444Thr | |
| ENST00000637736.1:c.1189G>A | ENSP00000489861.1:p.Ala397Thr | |
| ENST00000637769.1:c.1330G>A | ENSP00000489778.1:p.Ala444Thr | |
| ENST00000637927.1:c.1333G>A | ENSP00000489715.1:p.Ala445Thr | |
| ENST00000637966.1:n.1183G>A | ||
| ENST00000638009.2:c.1330G>A | ENSP00000489913.1:p.Ala444Thr | |
| ENST00000638029.1:c.1330G>A | ENSP00000489829.1:p.Ala444Thr | |
| ENST00000664864.1:c.1525G>A | ENSP00000499449.1:p.Ala509Thr | |
| ENST00000360228.9:c.1327G>A | ENSP00000353362.5:p.Ala443Thr | |
| ENST00000573710.6:c.1330G>A | ENSP00000460092.2:p.Ala444Thr | |
| ENST00000614285.4:c.1330G>A | ENSP00000479983.1:p.Ala444Thr | |
| NM_000068.3:c.1330G>A | NP_000059.3:p.Ala444Thr | |
| NM_001127221.1:c.1330G>A , LRG_7t1:c.1330G>A | NP_001120693.1:p.Ala444Thr | |
| NM_001127222.1:c.1327G>A | NP_001120694.1:p.Ala443Thr | |
| NM_001174080.1:c.1330G>A | NP_001167551.1:p.Ala444Thr | |
| NM_023035.2:c.1330G>A | NP_075461.2:p.Ala444Thr | |
| NM_000068.4:c.1330G>A | NP_000059.3:p.Ala444Thr | |
| NM_001127222.2:c.1327G>A MANE Select | NP_001120694.1:p.Ala443Thr | |
| NM_001174080.2:c.1330G>A | NP_001167551.1:p.Ala444Thr | |
| NM_023035.3:c.1330G>A | NP_075461.2:p.Ala444Thr | |
| NM_001127221.2:c.1330G>A | NP_001120693.1:p.Ala444Thr |