Linked Data
ClinVar Variation Id:
2449729
ClinVar RCV Id:
RCV003171726
dbSNP Id:
rs2125436028
gnomAD v4:
3-30672263-C-T
MyVariant Identifiers:
chr3:g.30713755C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.30672263C>T , CM000665.2:g.30672263C>T | GRCh38 |
| NC_000003.11:g.30713755C>T , CM000665.1:g.30713755C>T | GRCh37 |
| NC_000003.10:g.30688759C>T | NCBI36 |
| NG_007490.1:g.70762C>T , LRG_779:g.70762C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295754.10:c.1080C>T MANE Select | ENSP00000295754.5:p.His360= | |
| ENST00000672866.1:n.2676C>T | ||
| ENST00000295754.9:c.1080C>T | ENSP00000295754.5:p.His360= | |
| ENST00000359013.4:c.1155C>T | ENSP00000351905.4:p.His385= | |
| NM_001024847.2:c.1155C>T , LRG_779t1:c.1155C>T | NP_001020018.1:p.His385= | |
| NM_003242.5:c.1080C>T | NP_003233.4:p.His360= | |
| XM_011534043.1:c.1107C>T | XP_011532345.1:p.His369= | |
| XM_011534044.1:c.1032C>T | XP_011532346.1:p.His344= | |
| XM_011534045.1:c.975C>T | XP_011532347.1:p.His325= | |
| XM_011534043.2:c.1107C>T | XP_011532345.1:p.His369= | |
| XM_011534045.3:c.975C>T | XP_011532347.1:p.His325= | |
| XM_017007106.1:c.975C>T | XP_016862595.1:p.His325= | |
| NM_003242.6:c.1080C>T MANE Select | NP_003233.4:p.His360= |