Linked Data
ClinVar Variation Id:
422133
dbSNP Id:
rs372017604
ExAC:
19:13395925 T / C
gnomAD v2:
19-13395925-T-C
gnomAD v3:
19-13285111-T-C
gnomAD v4:
19-13285111-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.13285111T>C , CM000681.2:g.13285111T>C | GRCh38 |
| NC_000019.9:g.13395925T>C , CM000681.1:g.13395925T>C | GRCh37 |
| NC_000019.8:g.13256925T>C | NCBI36 |
| NG_011569.1:g.226350A>G , LRG_7:g.226350A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360228.11:c.3649A>G MANE Select | ENSP00000353362.5:p.Met1217Val | |
| ENST00000573710.7:c.3655A>G | ENSP00000460092.3:p.Met1219Val | |
| ENST00000635727.1:c.3652A>G | ENSP00000490001.1:p.Met1218Val | |
| ENST00000635786.1:n.148A>G | ||
| ENST00000635895.1:c.3652A>G | ENSP00000490323.1:p.Met1218Val | |
| ENST00000635917.1:n.141A>G | ||
| ENST00000636012.1:c.3652A>G | ENSP00000490223.1:p.Met1218Val | |
| ENST00000636389.1:c.3652A>G | ENSP00000489992.1:p.Met1218Val | |
| ENST00000636549.1:c.3652A>G | ENSP00000490578.1:p.Met1218Val | |
| ENST00000637004.1:n.115A>G | ||
| ENST00000637276.1:c.3652A>G | ENSP00000489777.1:p.Met1218Val | |
| ENST00000637432.1:c.3661A>G | ENSP00000490617.1:p.Met1221Val | |
| ENST00000637736.1:c.3511A>G | ENSP00000489861.1:p.Met1171Val | |
| ENST00000637769.1:c.3652A>G | ENSP00000489778.1:p.Met1218Val | |
| ENST00000637927.1:c.3655A>G | ENSP00000489715.1:p.Met1219Val | |
| ENST00000638009.2:c.3652A>G | ENSP00000489913.1:p.Met1218Val | |
| ENST00000638029.1:c.3661A>G | ENSP00000489829.1:p.Met1221Val | |
| ENST00000664864.1:c.3847A>G | ENSP00000499449.1:p.Met1283Val | |
| ENST00000360228.9:c.3649A>G | ENSP00000353362.5:p.Met1217Val | |
| ENST00000573710.6:c.3652A>G | ENSP00000460092.2:p.Met1218Val | |
| ENST00000614285.4:c.3661A>G | ENSP00000479983.1:p.Met1221Val | |
| NM_000068.3:c.3661A>G | NP_000059.3:p.Met1221Val | |
| NM_001127221.1:c.3652A>G , LRG_7t1:c.3652A>G | NP_001120693.1:p.Met1218Val | |
| NM_001127222.1:c.3649A>G | NP_001120694.1:p.Met1217Val | |
| NM_001174080.1:c.3652A>G | NP_001167551.1:p.Met1218Val | |
| NM_023035.2:c.3661A>G | NP_075461.2:p.Met1221Val | |
| NM_000068.4:c.3661A>G | NP_000059.3:p.Met1221Val | |
| NM_001127222.2:c.3649A>G MANE Select | NP_001120694.1:p.Met1217Val | |
| NM_001174080.2:c.3652A>G | NP_001167551.1:p.Met1218Val | |
| NM_023035.3:c.3661A>G | NP_075461.2:p.Met1221Val | |
| NM_001127221.2:c.3652A>G | NP_001120693.1:p.Met1218Val |