Linked Data
dbSNP Id:
rs762062072
ExAC:
15:68628079 T / C
gnomAD v2:
15-68628079-T-C
gnomAD v4:
15-68335741-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.68335741T>C , CM000677.2:g.68335741T>C | GRCh38 |
| NC_000015.9:g.68628079T>C , CM000677.1:g.68628079T>C | GRCh37 |
| NC_000015.8:g.66415133T>C | NCBI36 |
| NG_046911.1:g.101420A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000315757.9:c.1381A>G MANE Select | ENSP00000327290.7:p.Asn461Asp | |
| ENST00000315757.8:c.1381A>G | ENSP00000327290.7:p.Asn461Asp | |
| ENST00000423218.6:c.1381A>G | ENSP00000403392.2:p.Asn461Asp | |
| ENST00000566429.1:n.270A>G | ||
| ENST00000569346.5:n.360A>G | ||
| NM_001004439.1:c.1381A>G | NP_001004439.1:p.Asn461Asp | |
| XM_005254228.2:c.1075A>G | XP_005254285.1:p.Asn359Asp | |
| XM_011521363.1:c.1174A>G | XP_011519665.1:p.Asn392Asp | |
| XM_005254228.3:c.1075A>G | XP_005254285.1:p.Asn359Asp | |
| XM_011521363.2:c.1174A>G | XP_011519665.1:p.Asn392Asp | |
| NM_001004439.2:c.1381A>G MANE Select | NP_001004439.1:p.Asn461Asp |