Linked Data
ClinVar Variation Id:
448036
dbSNP Id:
rs755226061
ExAC:
4:88996055 C / T
gnomAD v2:
4-88996055-C-T
gnomAD v3:
4-88074903-C-T
gnomAD v4:
4-88074903-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.88074903C>T , CM000666.2:g.88074903C>T | GRCh38 |
| NC_000004.11:g.88996055C>T , CM000666.1:g.88996055C>T | GRCh37 |
| NC_000004.10:g.89215079C>T | NCBI36 |
| NG_008604.1:g.72236C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237596.7:c.2614C>T MANE Select | ENSP00000237596.2:p.Arg872Ter | |
| ENST00000237596.6:c.2614C>T | ENSP00000237596.2:p.Arg872Ter | |
| ENST00000502363.1:c.868C>T | ENSP00000425289.1:p.Arg290Ter | |
| ENST00000508588.5:c.868C>T | ENSP00000427131.1:p.Arg290Ter | |
| ENST00000511337.5:n.866C>T | ||
| ENST00000512858.1:n.1092C>T | ||
| NM_000297.3:c.2614C>T | NP_000288.1:p.Arg872Ter | |
| XM_011532028.1:c.2389C>T | XP_011530330.1:p.Arg797Ter | |
| XM_011532029.1:c.1894C>T | XP_011530331.1:p.Arg632Ter | |
| XM_011532030.1:c.1774C>T | XP_011530332.1:p.Arg592Ter | |
| NR_156488.1:n.2580C>T | ||
| XM_011532028.2:c.2389C>T | XP_011530330.1:p.Arg797Ter | |
| XM_011532030.2:c.1774C>T | XP_011530332.1:p.Arg592Ter | |
| NM_000297.4:c.2614C>T MANE Select | NP_000288.1:p.Arg872Ter | |
| NR_156488.2:n.2592C>T |