Linked Data
ClinVar Variation Id:
2081054
ClinVar RCV Id:
RCV002993988
dbSNP Id:
rs895300799
gnomAD v3:
5-13780878-A-G
gnomAD v4:
5-13780878-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13780878A>G , CM000667.2:g.13780878A>G | GRCh38 |
| NC_000005.9:g.13780987A>G , CM000667.1:g.13780987A>G | GRCh37 |
| NC_000005.8:g.13833987A>G | NCBI36 |
| NG_013081.1:g.168603T>C | |
| NG_013081.2:g.168603T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.8902T>C MANE Select | ENSP00000265104.4:p.Leu2968= | |
| ENST00000681290.1:c.8857T>C | ENSP00000505288.1:p.Leu2953= | |
| ENST00000265104.4:c.8902T>C | ENSP00000265104.4:p.Leu2968= | |
| NM_001369.2:c.8902T>C | NP_001360.1:p.Leu2968= | |
| XM_005248262.2:c.8857T>C | XP_005248319.1:p.Leu2953= | |
| XM_011513990.1:c.8902T>C | XP_011512292.1:p.Leu2968= | |
| XR_925598.1:n.9028-3523T>C | ||
| XM_005248262.3:c.9010T>C | XP_005248319.2:p.Leu3004= | |
| XM_017009177.1:c.9010T>C | XP_016864666.1:p.Leu3004= | |
| XM_017009178.1:c.7915T>C | XP_016864667.1:p.Leu2639= | |
| XM_017009179.2:c.7915T>C | XP_016864668.1:p.Leu2639= | |
| XM_017009180.1:c.9010T>C | XP_016864669.1:p.Leu3004= | |
| XM_017009181.1:c.9010T>C | XP_016864670.1:p.Leu3004= | |
| XM_017009182.1:c.9010T>C | XP_016864671.1:p.Leu3004= | |
| XM_017009183.1:c.9010T>C | XP_016864672.1:p.Leu3004= | |
| XM_017009184.1:c.9010T>C | XP_016864673.1:p.Leu3004= | |
| XM_017009185.1:c.4099T>C | XP_016864674.1:p.Leu1367= | |
| XM_017009186.1:c.3652T>C | XP_016864675.1:p.Leu1218= | |
| XM_017009188.1:c.2989T>C | XP_016864677.1:p.Leu997= | |
| XM_024454388.1:c.7915T>C | XP_024310156.1:p.Leu2639= | |
| XM_024454389.1:c.7504T>C | XP_024310157.1:p.Leu2502= | |
| XR_001742034.1:n.8946-3523T>C | ||
| XR_001742035.1:n.8946-3523T>C | ||
| NM_001369.3:c.8902T>C MANE Select | NP_001360.1:p.Leu2968= |