Linked Data
dbSNP Id:
rs2306023
ExAC:
15:68628143 C / T
gnomAD v2:
15-68628143-C-T
gnomAD v3:
15-68335805-C-T
gnomAD v4:
15-68335805-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.68335805C>T , CM000677.2:g.68335805C>T | GRCh38 |
| NC_000015.9:g.68628143C>T , CM000677.1:g.68628143C>T | GRCh37 |
| NC_000015.8:g.66415197C>T | NCBI36 |
| NG_046911.1:g.101356G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000315757.9:c.1317G>A MANE Select | ENSP00000327290.7:p.Arg439= | |
| ENST00000315757.8:c.1317G>A | ENSP00000327290.7:p.Arg439= | |
| ENST00000423218.6:c.1317G>A | ENSP00000403392.2:p.Arg439= | |
| ENST00000566429.1:n.206G>A | ||
| ENST00000569346.5:n.296G>A | ||
| NM_001004439.1:c.1317G>A | NP_001004439.1:p.Arg439= | |
| XM_005254228.2:c.1011G>A | XP_005254285.1:p.Arg337= | |
| XM_011521363.1:c.1110G>A | XP_011519665.1:p.Arg370= | |
| XM_005254228.3:c.1011G>A | XP_005254285.1:p.Arg337= | |
| XM_011521363.2:c.1110G>A | XP_011519665.1:p.Arg370= | |
| NM_001004439.2:c.1317G>A MANE Select | NP_001004439.1:p.Arg439= |