Linked Data
ClinVar Variation Id:
258060
dbSNP Id:
rs377367981
ExAC:
5:13807843 G / C
gnomAD v2:
5-13807843-G-C
gnomAD v3:
5-13807734-G-C
gnomAD v4:
5-13807734-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13807734G>C , CM000667.2:g.13807734G>C | GRCh38 |
| NC_000005.9:g.13807843G>C , CM000667.1:g.13807843G>C | GRCh37 |
| NC_000005.8:g.13860843G>C | NCBI36 |
| NG_013081.1:g.141747C>G | |
| NG_013081.2:g.141747C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.7753-9C>G MANE Select | ENSP00000265104.4:n.7753-9C>G | |
| ENST00000681290.1:c.7708-9C>G | ENSP00000505288.1:n.7708-9C>G | |
| ENST00000265104.4:c.7753-9C>G | ENSP00000265104.4:n.7753-9C>G | |
| ENST00000512443.1:n.609-9C>G | ||
| NM_001369.2:c.7753-9C>G | NP_001360.1:n.7753-9C>G | |
| XM_005248262.2:c.7708-9C>G | XP_005248319.1:n.7708-9C>G | |
| XM_011513990.1:c.7753-9C>G | XP_011512292.1:n.7753-9C>G | |
| XR_925598.1:n.7960-9C>G | ||
| XM_005248262.3:c.7861-9C>G | XP_005248319.2:n.7861-9C>G | |
| XM_017009177.1:c.7861-9C>G | XP_016864666.1:n.7861-9C>G | |
| XM_017009178.1:c.6766-9C>G | XP_016864667.1:n.6766-9C>G | |
| XM_017009179.2:c.6766-9C>G | XP_016864668.1:n.6766-9C>G | |
| XM_017009180.1:c.7861-9C>G | XP_016864669.1:n.7861-9C>G | |
| XM_017009181.1:c.7861-9C>G | XP_016864670.1:n.7861-9C>G | |
| XM_017009182.1:c.7861-9C>G | XP_016864671.1:n.7861-9C>G | |
| XM_017009183.1:c.7861-9C>G | XP_016864672.1:n.7861-9C>G | |
| XM_017009184.1:c.7861-9C>G | XP_016864673.1:n.7861-9C>G | |
| XM_017009185.1:c.2950-9C>G | XP_016864674.1:n.2950-9C>G | |
| XM_017009186.1:c.2503-9C>G | XP_016864675.1:n.2503-9C>G | |
| XM_017009187.1:c.7861-9C>G | XP_016864676.1:n.7861-9C>G | |
| XM_017009188.1:c.1840-9C>G | XP_016864677.1:n.1840-9C>G | |
| XM_024454388.1:c.6766-9C>G | XP_024310156.1:n.6766-9C>G | |
| XM_024454389.1:c.6355-9C>G | XP_024310157.1:n.6355-9C>G | |
| XR_001742034.1:n.7878-9C>G | ||
| XR_001742035.1:n.7878-9C>G | ||
| NM_001369.3:c.7753-9C>G MANE Select | NP_001360.1:n.7753-9C>G |