Linked Data
ClinVar Variation Id:
351205
dbSNP Id:
rs150793327
ExAC:
5:13900371 C / G
gnomAD v2:
5-13900371-C-G
gnomAD v3:
5-13900262-C-G
gnomAD v4:
5-13900262-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13900262C>G , CM000667.2:g.13900262C>G | GRCh38 |
| NC_000005.9:g.13900371C>G , CM000667.1:g.13900371C>G | GRCh37 |
| NC_000005.8:g.13953371C>G | NCBI36 |
| NG_013081.1:g.49219G>C | |
| NG_013081.2:g.49219G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.2203G>C MANE Select | ENSP00000265104.4:p.Ala735Pro | |
| ENST00000681290.1:c.2158G>C | ENSP00000505288.1:p.Ala720Pro | |
| ENST00000265104.4:c.2203G>C | ENSP00000265104.4:p.Ala735Pro | |
| NM_001369.2:c.2203G>C | NP_001360.1:p.Ala735Pro | |
| XM_005248262.2:c.2158G>C | XP_005248319.1:p.Ala720Pro | |
| XM_011513990.1:c.2203G>C | XP_011512292.1:p.Ala735Pro | |
| XR_925598.1:n.2410G>C | ||
| XM_005248262.3:c.2311G>C | XP_005248319.2:p.Ala771Pro | |
| XM_017009177.1:c.2311G>C | XP_016864666.1:p.Ala771Pro | |
| XM_017009178.1:c.1216G>C | XP_016864667.1:p.Ala406Pro | |
| XM_017009179.2:c.1216G>C | XP_016864668.1:p.Ala406Pro | |
| XM_017009180.1:c.2311G>C | XP_016864669.1:p.Ala771Pro | |
| XM_017009181.1:c.2311G>C | XP_016864670.1:p.Ala771Pro | |
| XM_017009182.1:c.2311G>C | XP_016864671.1:p.Ala771Pro | |
| XM_017009183.1:c.2311G>C | XP_016864672.1:p.Ala771Pro | |
| XM_017009184.1:c.2311G>C | XP_016864673.1:p.Ala771Pro | |
| XM_017009187.1:c.2311G>C | XP_016864676.1:p.Ala771Pro | |
| XM_024454388.1:c.1216G>C | XP_024310156.1:p.Ala406Pro | |
| XM_024454389.1:c.805G>C | XP_024310157.1:p.Ala269Pro | |
| XR_001742034.1:n.2328G>C | ||
| XR_001742035.1:n.2328G>C | ||
| NM_001369.3:c.2203G>C MANE Select | NP_001360.1:p.Ala735Pro |