Linked Data
ClinVar Variation Id:
1960288
ClinVar RCV Id:
RCV002706404
dbSNP Id:
rs570495195
ExAC:
1:245027159 C / T
gnomAD v4:
1-244863857-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.244863857C>T , CM000663.2:g.244863857C>T | GRCh38 |
| NC_000001.10:g.245027159C>T , CM000663.1:g.245027159C>T | GRCh37 |
| NC_000001.9:g.243093782C>T | NCBI36 |
| NG_042184.1:g.5669G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000704074.1:c.129G>A | ||
| ENST00000283179.14:c.451G>A | ENSP00000283179.10:p.Gly151Ser | |
| ENST00000444376.7:c.451G>A | ENSP00000393151.2:p.Gly151Ser | |
| ENST00000476241.2:n.636G>A | ||
| ENST00000638475.1:c.235G>A | ENSP00000491305.1:p.Gly79Ser | |
| ENST00000638952.1:n.682G>A | ||
| ENST00000640218.2:c.451G>A MANE Select | ENSP00000491215.1:p.Gly151Ser | |
| ENST00000640306.1:c.451G>A | ENSP00000491685.1:p.Gly151Ser | |
| ENST00000640440.1:c.151G>A | ENSP00000491263.1:p.Gly51Ser | |
| ENST00000649899.1:n.675G>A | ||
| ENST00000283179.13:c.451G>A | ENSP00000283179.9:p.Gly151Ser | |
| ENST00000444376.6:c.451G>A | ENSP00000393151.2:p.Gly151Ser | |
| ENST00000476241.1:n.635G>A | ||
| NM_004501.3:c.451G>A | NP_004492.2:p.Gly151Ser | |
| NM_031844.2:c.451G>A | NP_114032.2:p.Gly151Ser | |
| NM_031844.3:c.451G>A MANE Select | NP_114032.2:p.Gly151Ser |