Linked Data
ClinVar Variation Id:
407242
dbSNP Id:
rs1060501464
gnomAD v2:
5-13735276-G-A
gnomAD v4:
5-13735167-G-A
COSMIC:
COSM395284
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13735167G>A , CM000667.2:g.13735167G>A | GRCh38 |
| NC_000005.9:g.13735276G>A , CM000667.1:g.13735276G>A | GRCh37 |
| NC_000005.8:g.13788276G>A | NCBI36 |
| NG_013081.1:g.214314C>T | |
| NG_013081.2:g.214314C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.11725C>T MANE Select | ENSP00000265104.4:p.Arg3909Ter | |
| ENST00000681290.1:c.11680C>T | ENSP00000505288.1:p.Arg3894Ter | |
| ENST00000265104.4:c.11725C>T | ENSP00000265104.4:p.Arg3909Ter | |
| NM_001369.2:c.11725C>T | NP_001360.1:p.Arg3909Ter | |
| XM_005248262.2:c.11680C>T | XP_005248319.1:p.Arg3894Ter | |
| XM_005248262.3:c.11833C>T | XP_005248319.2:p.Arg3945Ter | |
| XM_017009177.1:c.11833C>T | XP_016864666.1:p.Arg3945Ter | |
| XM_017009178.1:c.10738C>T | XP_016864667.1:p.Arg3580Ter | |
| XM_017009179.2:c.10738C>T | XP_016864668.1:p.Arg3580Ter | |
| XM_017009180.1:c.11833C>T | XP_016864669.1:p.Arg3945Ter | |
| XM_017009181.1:c.11833C>T | XP_016864670.1:p.Arg3945Ter | |
| XM_017009185.1:c.6922C>T | XP_016864674.1:p.Arg2308Ter | |
| XM_017009186.1:c.6475C>T | XP_016864675.1:p.Arg2159Ter | |
| XM_017009188.1:c.5812C>T | XP_016864677.1:p.Arg1938Ter | |
| XM_024454388.1:c.10738C>T | XP_024310156.1:p.Arg3580Ter | |
| XM_024454389.1:c.10327C>T | XP_024310157.1:p.Arg3443Ter | |
| NM_001369.3:c.11725C>T MANE Select | NP_001360.1:p.Arg3909Ter |