Linked Data
ClinVar Variation Id:
489087
dbSNP Id:
rs1462559161
gnomAD v3:
10-95606857-G-A
gnomAD v4:
10-95606857-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.95606857G>A , CM000672.2:g.95606857G>A | GRCh38 |
| NC_000010.10:g.97366614G>A , CM000672.1:g.97366614G>A | GRCh37 |
| NC_000010.9:g.97356604G>A | NCBI36 |
| NG_012258.1:g.54954C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371224.7:c.2293C>T MANE Select | ENSP00000360268.2:p.Arg765Ter | |
| ENST00000371221.3:c.2287C>T | ENSP00000360265.3:p.Arg763Ter | |
| ENST00000371224.6:c.2293C>T | ENSP00000360268.2:p.Arg765Ter | |
| NM_001017423.1:c.2287C>T | NP_001017423.1:p.Arg763Ter | |
| NM_002860.3:c.2293C>T | NP_002851.2:p.Arg765Ter | |
| XM_006717933.1:c.2293C>T | XP_006717996.1:p.Arg765Ter | |
| XM_011540001.1:c.1960C>T | XP_011538303.1:p.Arg654Ter | |
| NM_001323412.1:c.1960C>T | NP_001310341.1:p.Arg654Ter | |
| NM_001323413.1:c.2293C>T | NP_001310342.1:p.Arg765Ter | |
| NM_001323414.1:c.2293C>T | NP_001310343.1:p.Arg765Ter | |
| NM_001323415.1:c.2287C>T | NP_001310344.1:p.Arg763Ter | |
| NM_001323416.1:c.1960C>T | NP_001310345.1:p.Arg654Ter | |
| NM_001323417.1:c.2188C>T | NP_001310346.1:p.Arg730Ter | |
| NM_001323418.1:c.1954C>T | NP_001310347.1:p.Arg652Ter | |
| NM_001323419.1:c.1657C>T | NP_001310348.1:p.Arg553Ter | |
| XM_024448094.1:c.2395C>T | XP_024303862.1:p.Arg799Ter | |
| XM_024448095.1:c.2395C>T | XP_024303863.1:p.Arg799Ter | |
| XM_024448096.1:c.2389C>T | XP_024303864.1:p.Arg797Ter | |
| XM_024448097.1:c.2062C>T | XP_024303865.1:p.Arg688Ter | |
| NM_002860.4:c.2293C>T MANE Select | NP_002851.2:p.Arg765Ter | |
| NM_001017423.2:c.2287C>T | NP_001017423.1:p.Arg763Ter | |
| NM_001323412.2:c.1960C>T | NP_001310341.1:p.Arg654Ter | |
| NM_001323413.2:c.2293C>T | NP_001310342.1:p.Arg765Ter | |
| NM_001323414.2:c.2293C>T | NP_001310343.1:p.Arg765Ter | |
| NM_001323415.2:c.2287C>T | NP_001310344.1:p.Arg763Ter | |
| NM_001323416.2:c.1960C>T | NP_001310345.1:p.Arg654Ter | |
| NM_001323417.2:c.2188C>T | NP_001310346.1:p.Arg730Ter | |
| NM_001323418.2:c.1954C>T | NP_001310347.1:p.Arg652Ter | |
| NM_001323419.2:c.1657C>T | NP_001310348.1:p.Arg553Ter |