Linked Data
ClinVar Variation Id:
2979151
ClinVar RCV Id:
RCV003831781
dbSNP Id:
rs769688446
gnomAD v3:
20-49373020-C-T
gnomAD v4:
20-49373020-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.49373020C>T , CM000682.2:g.49373020C>T | GRCh38 |
| NC_000020.10:g.47989557C>T , CM000682.1:g.47989557C>T | GRCh37 |
| NC_000020.9:g.47422964C>T | NCBI36 |
| NG_041781.1:g.114625G>A | |
| NG_041781.2:g.114625G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371741.6:c.2540G>A MANE Select | ENSP00000360806.3:p.Gly847Glu | |
| ENST00000635878.1:c.97-73637G>A | ENSP00000489908.1:n.97-73637G>A | |
| ENST00000637131.1:c.84G>A | ||
| ENST00000637341.1:n.206+40996C>T | ||
| ENST00000371741.5:c.2540G>A | ENSP00000360806.3:p.Gly847Glu | |
| ENST00000635465.1:c.2540G>A | ENSP00000489193.1:p.Gly847Glu | |
| NM_004975.2:c.2540G>A | NP_004966.1:p.Gly847Glu | |
| XM_006723784.2:c.2540G>A | XP_006723847.1:p.Gly847Glu | |
| XM_011528799.1:c.2540G>A | XP_011527101.1:p.Gly847Glu | |
| NM_004975.3:c.2540G>A | NP_004966.1:p.Gly847Glu | |
| XM_006723784.3:c.2540G>A | XP_006723847.1:p.Gly847Glu | |
| XM_011528799.2:c.2540G>A | XP_011527101.1:p.Gly847Glu | |
| XR_001754659.1:n.156+40996C>T | ||
| NM_004975.4:c.2540G>A MANE Select | NP_004966.1:p.Gly847Glu |