Linked Data
ClinVar Variation Id:
1087739
dbSNP Id:
rs994129583
MyVariant Identifiers:
chr13:g.49033909C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48459773C>T , CM000675.2:g.48459773C>T | GRCh38 |
| NC_000013.10:g.49033909C>T , CM000675.1:g.49033909C>T | GRCh37 |
| NC_000013.9:g.47931910C>T | NCBI36 |
| NG_009009.1:g.161027C>T , LRG_517:g.161027C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.2046C>T MANE Select | ENSP00000267163.4:p.Thr682= | |
| ENST00000643064.1:c.194+78330C>T | ||
| ENST00000650461.1:c.2046C>T | ENSP00000497193.1:p.Thr682= | |
| ENST00000267163.4:c.2046C>T | ENSP00000267163.4:p.Thr682= | |
| NM_000321.2:c.2046C>T , LRG_517t1:c.2046C>T | NP_000312.2:p.Thr682= | |
| XM_011535171.1:c.1785C>T | XP_011533473.1:p.Thr595= | |
| XM_011535171.2:c.1785C>T | XP_011533473.1:p.Thr595= | |
| NM_000321.3:c.2046C>T MANE Select | NP_000312.2:p.Thr682= |