Linked Data
dbSNP Id:
rs769757873
ExAC:
1:218610778 T / C
gnomAD v2:
1-218610778-T-C
gnomAD v4:
1-218437436-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.218437436T>C , CM000663.2:g.218437436T>C | GRCh38 |
| NC_000001.10:g.218610778T>C , CM000663.1:g.218610778T>C | GRCh37 |
| NC_000001.9:g.216677401T>C | NCBI36 |
| NG_027721.1:g.97103T>C | |
| NG_027721.2:g.97103T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366930.9:c.1026T>C MANE Select | ENSP00000355897.4:p.Asn342= | |
| ENST00000366929.4:c.1110T>C | ENSP00000355896.4:p.Asn370= | |
| ENST00000366930.8:c.1026T>C | ENSP00000355897.4:p.Asn342= | |
| ENST00000479322.1:n.510T>C | ||
| NM_001135599.2:c.1110T>C | NP_001129071.1:p.Asn370= | |
| NM_003238.3:c.1026T>C | NP_003229.1:p.Asn342= | |
| NM_001135599.3:c.1110T>C | NP_001129071.1:p.Asn370= | |
| NM_003238.4:c.1026T>C | NP_003229.1:p.Asn342= | |
| NR_138148.1:n.2329T>C | ||
| NR_138149.1:n.2413T>C | ||
| NM_003238.5:c.1026T>C | NP_003229.1:p.Asn342= | |
| NM_003238.6:c.1026T>C MANE Select | NP_003229.1:p.Asn342= | |
| NM_001135599.4:c.1110T>C | NP_001129071.1:p.Asn370= | |
| NR_138148.2:n.2277T>C | ||
| NR_138149.2:n.2361T>C |