Linked Data
ClinVar Variation Id:
1507780
ClinVar RCV Id:
RCV002013629
dbSNP Id:
rs778312386
gnomAD v2:
5-13776604-A-G
gnomAD v3:
5-13776495-A-G
gnomAD v4:
5-13776495-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13776495A>G , CM000667.2:g.13776495A>G | GRCh38 |
| NC_000005.9:g.13776604A>G , CM000667.1:g.13776604A>G | GRCh37 |
| NC_000005.8:g.13829604A>G | NCBI36 |
| NG_013081.1:g.172986T>C | |
| NG_013081.2:g.172986T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.9317T>C MANE Select | ENSP00000265104.4:p.Ile3106Thr | |
| ENST00000681290.1:c.9272T>C | ENSP00000505288.1:p.Ile3091Thr | |
| ENST00000265104.4:c.9317T>C | ENSP00000265104.4:p.Ile3106Thr | |
| NM_001369.2:c.9317T>C | NP_001360.1:p.Ile3106Thr | |
| XM_005248262.2:c.9272T>C | XP_005248319.1:p.Ile3091Thr | |
| XM_005248262.3:c.9425T>C | XP_005248319.2:p.Ile3142Thr | |
| XM_017009177.1:c.9425T>C | XP_016864666.1:p.Ile3142Thr | |
| XM_017009178.1:c.8330T>C | XP_016864667.1:p.Ile2777Thr | |
| XM_017009179.2:c.8330T>C | XP_016864668.1:p.Ile2777Thr | |
| XM_017009180.1:c.9425T>C | XP_016864669.1:p.Ile3142Thr | |
| XM_017009181.1:c.9425T>C | XP_016864670.1:p.Ile3142Thr | |
| XM_017009182.1:c.9425T>C | XP_016864671.1:p.Ile3142Thr | |
| XM_017009183.1:c.9425T>C | XP_016864672.1:p.Ile3142Thr | |
| XM_017009185.1:c.4514T>C | XP_016864674.1:p.Ile1505Thr | |
| XM_017009186.1:c.4067T>C | XP_016864675.1:p.Ile1356Thr | |
| XM_017009188.1:c.3404T>C | XP_016864677.1:p.Ile1135Thr | |
| XM_024454388.1:c.8330T>C | XP_024310156.1:p.Ile2777Thr | |
| XM_024454389.1:c.7919T>C | XP_024310157.1:p.Ile2640Thr | |
| NM_001369.3:c.9317T>C MANE Select | NP_001360.1:p.Ile3106Thr |