Linked Data
dbSNP Id:
rs2135598153
gnomAD v4:
10-102504251-A-C
MyVariant Identifiers:
chr10:g.104264008A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102504251A>C , CM000672.2:g.102504251A>C | GRCh38 |
| NC_000010.10:g.104264008A>C , CM000672.1:g.104264008A>C | GRCh37 |
| NC_000010.9:g.104253998A>C | NCBI36 |
| NG_011901.1:g.3505T>G | |
| NG_021338.1:g.5290A>C , LRG_521:g.5290A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369902.8:c.99A>C MANE Select | ENSP00000358918.4:p.Gly33= | |
| ENST00000369899.6:c.99A>C | ENSP00000358915.2:p.Gly33= | |
| ENST00000369902.7:c.99A>C | ENSP00000358918.3:p.Gly33= | |
| ENST00000423559.2:c.99A>C | ENSP00000411597.2:p.Gly33= | |
| NM_001178133.1:c.99A>C | NP_001171604.1:p.Gly33= | |
| NM_016169.3:c.99A>C , LRG_521t1:c.99A>C | NP_057253.2:p.Gly33= | |
| XM_011539858.1:c.99A>C | XP_011538160.1:p.Gly33= | |
| XM_011539859.1:c.99A>C | XP_011538161.1:p.Gly33= | |
| XM_011539860.1:c.99A>C | XP_011538162.1:p.Gly33= | |
| XM_011539861.1:c.99A>C | XP_011538163.1:p.Gly33= | |
| XM_011539862.1:c.-117A>C | XP_011538164.1:n.-117A>C | |
| XM_011539863.1:c.8+1265A>C | XP_011538165.1:n.8+1265A>C | |
| XM_011539864.1:c.99A>C | XP_011538166.1:p.Gly33= | |
| XM_011539858.3:c.99A>C | XP_011538160.1:p.Gly33= | |
| XM_011539860.3:c.99A>C | XP_011538162.1:p.Gly33= | |
| XM_011539861.3:c.99A>C | XP_011538163.1:p.Gly33= | |
| XM_011539863.3:c.8+1265A>C | XP_011538165.1:n.8+1265A>C | |
| XM_011539864.3:c.99A>C | XP_011538166.1:p.Gly33= | |
| NM_001178133.2:c.99A>C | NP_001171604.1:p.Gly33= | |
| NM_016169.4:c.99A>C MANE Select | NP_057253.2:p.Gly33= |