Linked Data
dbSNP Id:
rs1763212948
gnomAD v4:
5-177403942-C-T
MyVariant Identifiers:
chr5:g.176830943C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.177403942C>T , CM000667.2:g.177403942C>T | GRCh38 |
| NC_000005.9:g.176830943C>T , CM000667.1:g.176830943C>T | GRCh37 |
| NC_000005.8:g.176763549C>T | NCBI36 |
| NG_007568.1:g.10635G>A , LRG_145:g.10635G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696192.1:c.*833G>A (F12) | ENSP00000512476.1:n.*833G>A | |
| ENST00000696193.1:c.*1554G>A (F12) | ENSP00000512477.1:n.*1554G>A | |
| ENST00000696194.1:c.*757G>A (F12) | ENSP00000512478.1:n.*757G>A | |
| ENST00000696195.1:n.3970G>A (F12) | ||
| ENST00000696200.1:n.1270G>A (F12) | ||
| ENST00000696201.1:c.1167G>A (F12) | ENSP00000512482.1:p.Ala389= | |
| ENST00000253496.4:c.1167G>A (F12) MANE Select | ENSP00000253496.3:p.Ala389= | |
| ENST00000253496.3:c.1167G>A (F12) | ENSP00000253496.3:p.Ala389= | |
| ENST00000502598.5:c.-45+416C>T (GRK6) | ENSP00000422873.1:n.-45+416C>T | |
| ENST00000502854.5:n.426G>A (F12) | ||
| ENST00000503736.1:n.539G>A (F12) | ||
| ENST00000510358.5:n.531G>A (F12) | ||
| NM_000505.3:c.1167G>A , LRG_145t1:c.1167G>A (F12) | NP_000496.2:p.Ala389= | |
| XM_011534461.1:c.1167G>A (F12) | XP_011532763.1:p.Ala389= | |
| XM_011534462.1:c.831G>A (F12) | XP_011532764.1:p.Ala277= | |
| XM_011534462.2:c.831G>A (F12) | XP_011532764.1:p.Ala277= | |
| XM_017009773.2:c.1416+6868C>T (SLC34A1) | XP_016865262.1:n.1416+6868C>T | |
| NM_000505.4:c.1167G>A (F12) MANE Select | NP_000496.2:p.Ala389= |