Linked Data
ClinVar Variation Id:
387527
ClinVar RCV Id:
RCV000434641
RCV000540512
RCV000766720
RCV001125757
RCV001125756
RCV001127851
RCV002279198
dbSNP Id:
rs72648327
ExAC:
17:48272643 G / A
gnomAD v2:
17-48272643-G-A
gnomAD v3:
17-50195282-G-A
gnomAD v4:
17-50195282-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50195282G>A , CM000679.2:g.50195282G>A | GRCh38 |
| NC_000017.10:g.48272643G>A , CM000679.1:g.48272643G>A | GRCh37 |
| NC_000017.9:g.45627642G>A | NCBI36 |
| NG_007400.1:g.11358C>T , LRG_1:g.11358C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225964.10:c.1249C>T MANE Select | ENSP00000225964.6:p.Pro417Ser | |
| ENST00000225964.9:c.1249C>T | ENSP00000225964.5:p.Pro417Ser | |
| ENST00000471344.1:n.193C>T | ||
| NM_000088.3:c.1249C>T , LRG_1t1:c.1249C>T | NP_000079.2:p.Pro417Ser | |
| XM_005257058.3:c.1249C>T | XP_005257115.2:p.Pro417Ser | |
| XM_005257059.3:c.957+1032C>T | XP_005257116.2:n.957+1032C>T | |
| XM_011524341.1:c.1051C>T | XP_011522643.1:p.Pro351Ser | |
| XM_005257058.4:c.1249C>T | XP_005257115.2:p.Pro417Ser | |
| XM_005257059.4:c.957+1032C>T | XP_005257116.2:n.957+1032C>T | |
| NM_000088.4:c.1249C>T MANE Select | NP_000079.2:p.Pro417Ser |