Linked Data
ClinVar Variation Id:
265005
dbSNP Id:
rs114863111
ExAC:
2:215852458 G / A
gnomAD v2:
2-215852458-G-A
gnomAD v3:
2-214987734-G-A
gnomAD v4:
2-214987734-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214987734G>A , CM000664.2:g.214987734G>A | GRCh38 |
| NC_000002.11:g.215852458G>A , CM000664.1:g.215852458G>A | GRCh37 |
| NC_000002.10:g.215560703G>A | NCBI36 |
| NG_007074.1:g.155694C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272895.12:c.3889C>T MANE Select | ENSP00000272895.7:p.Arg1297Ter | |
| ENST00000272895.11:c.3889C>T | ENSP00000272895.7:p.Arg1297Ter | |
| ENST00000389661.4:c.2935C>T | ENSP00000374312.4:p.Arg979Ter | |
| NM_015657.3:c.2935C>T | NP_056472.2:p.Arg979Ter | |
| NM_173076.2:c.3889C>T | NP_775099.2:p.Arg1297Ter | |
| NR_103740.1:n.4189C>T | ||
| XM_011510951.1:c.3889C>T | XP_011509253.1:p.Arg1297Ter | |
| XM_011510952.1:c.3889C>T | XP_011509254.1:p.Arg1297Ter | |
| XM_011510951.2:c.3889C>T | XP_011509253.1:p.Arg1297Ter | |
| NM_173076.3:c.3889C>T MANE Select | NP_775099.2:p.Arg1297Ter | |
| NR_103740.2:n.4387C>T | ||
| NM_015657.4:c.2935C>T | NP_056472.2:p.Arg979Ter |