Linked Data
ClinVar Variation Id:
543907
dbSNP Id:
rs574133875
ExAC:
3:30686270 C / T
gnomAD v2:
3-30686270-C-T
gnomAD v3:
3-30644778-C-T
gnomAD v4:
3-30644778-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.30644778C>T , CM000665.2:g.30644778C>T | GRCh38 |
| NC_000003.11:g.30686270C>T , CM000665.1:g.30686270C>T | GRCh37 |
| NC_000003.10:g.30661274C>T | NCBI36 |
| NG_007490.1:g.43277C>T , LRG_779:g.43277C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295754.10:c.126C>T MANE Select | ENSP00000295754.5:p.Asn42= | |
| ENST00000672866.1:n.1722C>T | ||
| ENST00000673250.1:n.250C>T | ||
| ENST00000295754.9:c.126C>T | ENSP00000295754.5:p.Asn42= | |
| ENST00000359013.4:c.201C>T | ENSP00000351905.4:p.Asn67= | |
| NM_001024847.2:c.201C>T , LRG_779t1:c.201C>T | NP_001020018.1:p.Asn67= | |
| NM_003242.5:c.126C>T | NP_003233.4:p.Asn42= | |
| XM_011534043.1:c.153C>T | XP_011532345.1:p.Asn51= | |
| XM_011534044.1:c.78C>T | XP_011532346.1:p.Asn26= | |
| XM_011534045.1:c.21C>T | XP_011532347.1:p.Asn7= | |
| XM_011534043.2:c.153C>T | XP_011532345.1:p.Asn51= | |
| XM_011534045.3:c.21C>T | XP_011532347.1:p.Asn7= | |
| XM_017007106.1:c.21C>T | XP_016862595.1:p.Asn7= | |
| NM_003242.6:c.126C>T MANE Select | NP_003233.4:p.Asn42= |