Linked Data
ClinVar Variation Id:
1158764
ClinVar RCV Id:
RCV001502289
dbSNP Id:
rs755073295
gnomAD v2:
17-48271394-G-A
gnomAD v3:
17-50194033-G-A
gnomAD v4:
17-50194033-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50194033G>A , CM000679.2:g.50194033G>A | GRCh38 |
| NC_000017.10:g.48271394G>A , CM000679.1:g.48271394G>A | GRCh37 |
| NC_000017.9:g.45626393G>A | NCBI36 |
| NG_007400.1:g.12607C>T , LRG_1:g.12607C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225964.10:c.1677C>T MANE Select | ENSP00000225964.6:p.Ala559= | |
| ENST00000225964.9:c.1677C>T | ENSP00000225964.5:p.Ala559= | |
| ENST00000463440.1:n.67C>T | ||
| ENST00000471344.1:n.709C>T | ||
| ENST00000476387.1:n.26C>T | ||
| NM_000088.3:c.1677C>T , LRG_1t1:c.1677C>T | NP_000079.2:p.Ala559= | |
| XM_005257058.3:c.1677C>T | XP_005257115.2:p.Ala559= | |
| XM_005257059.3:c.958-1340C>T | XP_005257116.2:n.958-1340C>T | |
| XM_011524341.1:c.1479C>T | XP_011522643.1:p.Ala493= | |
| XM_005257058.4:c.1677C>T | XP_005257115.2:p.Ala559= | |
| XM_005257059.4:c.958-1340C>T | XP_005257116.2:n.958-1340C>T | |
| NM_000088.4:c.1677C>T MANE Select | NP_000079.2:p.Ala559= |