Linked Data
ClinVar Variation Id:
2744949
ClinVar RCV Id:
RCV003535550
MyVariant Identifiers:
chr5:g.13876913T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13876804T>G , CM000667.2:g.13876804T>G | GRCh38 |
| NC_000005.9:g.13876913T>G , CM000667.1:g.13876913T>G | GRCh37 |
| NC_000005.8:g.13929913T>G | NCBI36 |
| NG_013081.1:g.72677A>C | |
| NG_013081.2:g.72677A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.3276A>C MANE Select | ENSP00000265104.4:p.Ile1092= | |
| ENST00000681290.1:c.3231A>C | ENSP00000505288.1:p.Ile1077= | |
| ENST00000265104.4:c.3276A>C | ENSP00000265104.4:p.Ile1092= | |
| NM_001369.2:c.3276A>C | NP_001360.1:p.Ile1092= | |
| XM_005248262.2:c.3231A>C | XP_005248319.1:p.Ile1077= | |
| XM_011513990.1:c.3276A>C | XP_011512292.1:p.Ile1092= | |
| XR_925598.1:n.3483A>C | ||
| XM_005248262.3:c.3384A>C | XP_005248319.2:p.Ile1128= | |
| XM_017009177.1:c.3384A>C | XP_016864666.1:p.Ile1128= | |
| XM_017009178.1:c.2289A>C | XP_016864667.1:p.Ile763= | |
| XM_017009179.2:c.2289A>C | XP_016864668.1:p.Ile763= | |
| XM_017009180.1:c.3384A>C | XP_016864669.1:p.Ile1128= | |
| XM_017009181.1:c.3384A>C | XP_016864670.1:p.Ile1128= | |
| XM_017009182.1:c.3384A>C | XP_016864671.1:p.Ile1128= | |
| XM_017009183.1:c.3384A>C | XP_016864672.1:p.Ile1128= | |
| XM_017009184.1:c.3384A>C | XP_016864673.1:p.Ile1128= | |
| XM_017009187.1:c.3384A>C | XP_016864676.1:p.Ile1128= | |
| XM_024454388.1:c.2289A>C | XP_024310156.1:p.Ile763= | |
| XM_024454389.1:c.1878A>C | XP_024310157.1:p.Ile626= | |
| XR_001742034.1:n.3401A>C | ||
| XR_001742035.1:n.3401A>C | ||
| NM_001369.3:c.3276A>C MANE Select | NP_001360.1:p.Ile1092= |