Linked Data
ClinVar Variation Id:
1608600
ClinVar RCV Id:
RCV002147554
dbSNP Id:
rs2151562365
MyVariant Identifiers:
chr16:g.89211676G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89145268G>C , CM000678.2:g.89145268G>C | GRCh38 |
| NC_000016.9:g.89211676G>C , CM000678.1:g.89211676G>C | GRCh37 |
| NC_000016.8:g.87739177G>C | NCBI36 |
| NG_031961.1:g.56460G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000317447.9:c.1368G>C | ENSP00000320646.4:p.Gly456= | |
| ENST00000614302.5:c.1368G>C MANE Select | ENSP00000479130.1:p.Gly456= | |
| ENST00000649953.1:c.1578G>C | ENSP00000497456.1:p.Gly526= | |
| ENST00000317447.8:c.1368G>C | ENSP00000320646.4:p.Gly456= | |
| ENST00000378345.8:c.573G>C | ENSP00000367596.4:p.Gly191= | |
| ENST00000406948.7:c.1368G>C | ENSP00000384627.3:p.Gly456= | |
| ENST00000537116.5:n.494G>C | ||
| ENST00000537155.1:n.108G>C | ||
| ENST00000542688.5:c.*112G>C | ENSP00000446281.1:n.*112G>C | |
| ENST00000544543.5:c.573G>C | ENSP00000442781.1:p.Gly191= | |
| ENST00000562204.1:n.341G>C | ||
| ENST00000614302.4:c.1368G>C | ENSP00000479130.1:p.Gly456= | |
| NM_001127214.3:c.1368G>C | NP_001120686.1:p.Gly456= | |
| NM_001243279.2:c.1368G>C | NP_001230208.1:p.Gly456= | |
| NM_001284316.1:c.573G>C | NP_001271245.1:p.Gly191= | |
| NM_174917.4:c.1368G>C | NP_777577.2:p.Gly456= | |
| NR_045667.2:n.494G>C | ||
| NR_104293.1:n.1802G>C | ||
| XM_005256293.1:c.1368G>C | XP_005256350.1:p.Gly456= | |
| XM_011522942.1:c.1368G>C | XP_011521244.1:p.Gly456= | |
| XM_011522943.1:c.1368G>C | XP_011521245.1:p.Gly456= | |
| XR_933239.1:n.1809G>C | ||
| XR_933240.1:n.1806G>C | ||
| XR_933241.1:n.1563G>C | ||
| NR_147928.1:n.1846G>C | ||
| NR_147929.1:n.1600G>C | ||
| XM_005256293.2:c.1368G>C | XP_005256350.1:p.Gly456= | |
| XM_017023018.1:c.1368G>C | XP_016878507.1:p.Gly456= | |
| XM_017023019.1:c.1368G>C | XP_016878508.1:p.Gly456= | |
| XM_017023020.2:c.-3737G>C | XP_016878509.1:n.-3737G>C | |
| XM_017023022.1:c.501G>C | XP_016878511.1:p.Gly167= | |
| XM_024450186.1:c.573G>C | XP_024305954.1:p.Gly191= | |
| XM_024450187.1:c.573G>C | XP_024305955.1:p.Gly191= | |
| XR_001751864.2:n.1615G>C | ||
| XR_001751865.1:n.1562G>C | ||
| XR_933240.3:n.1805G>C | ||
| NM_001127214.4:c.1368G>C | NP_001120686.1:p.Gly456= | |
| NM_001243279.3:c.1368G>C MANE Select | NP_001230208.1:p.Gly456= | |
| NM_001284316.2:c.573G>C | NP_001271245.1:p.Gly191= | |
| NM_174917.5:c.1368G>C | NP_777577.2:p.Gly456= | |
| NR_104293.2:n.1759G>C | ||
| NR_147928.2:n.1803G>C | ||
| NR_147929.2:n.1557G>C |