Linked Data
ClinVar Variation Id:
1135016
ClinVar RCV Id:
RCV001470151
dbSNP Id:
rs2135336464
MyVariant Identifiers:
chr11:g.108005039T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108134312T>C , CM000673.2:g.108134312T>C | GRCh38 |
| NC_000011.9:g.108005039T>C , CM000673.1:g.108005039T>C | GRCh37 |
| NC_000011.8:g.107510249T>C | NCBI36 |
| NG_009888.1:g.17782T>C | |
| NG_009888.2:g.22608T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265838.9:c.330T>C MANE Select | ENSP00000265838.4:p.Gly110= | |
| ENST00000671707.1:n.425T>C | ||
| ENST00000672008.1:c.314+16T>C | ENSP00000500499.1:n.314+16T>C | |
| ENST00000672031.1:c.330T>C | ENSP00000500463.1:p.Gly110= | |
| ENST00000672284.1:c.60T>C | ENSP00000500444.1:p.Gly20= | |
| ENST00000672354.1:c.330T>C | ENSP00000500490.1:p.Gly110= | |
| ENST00000672367.1:c.73-4586T>C | ENSP00000500209.1:n.73-4586T>C | |
| ENST00000672580.1:c.330T>C | ENSP00000500366.1:p.Gly110= | |
| ENST00000672907.1:c.120+2358T>C | ENSP00000500928.1:n.120+2358T>C | |
| ENST00000673000.1:n.418T>C | ||
| ENST00000673531.1:c.60T>C | ENSP00000500163.1:p.Gly20= | |
| ENST00000265838.8:c.330T>C | ENSP00000265838.4:p.Gly110= | |
| ENST00000299355.10:c.330T>C | ENSP00000299355.6:p.Gly110= | |
| ENST00000524833.5:n.370T>C | ||
| ENST00000527942.5:c.60T>C | ENSP00000433568.1:p.Gly20= | |
| ENST00000528370.1:c.136T>C | ||
| ENST00000531813.5:c.330T>C | ENSP00000435965.1:p.Gly110= | |
| NM_000019.3:c.330T>C | NP_000010.1:p.Gly110= | |
| XM_006718834.2:c.60T>C | XP_006718897.1:p.Gly20= | |
| XM_006718835.2:c.60T>C | XP_006718898.1:p.Gly20= | |
| XM_006718835.3:c.60T>C | XP_006718898.1:p.Gly20= | |
| XM_017017681.1:c.60T>C | XP_016873170.1:p.Gly20= | |
| XM_017017682.2:c.53T>C | XP_016873171.1:p.Val18Ala | |
| XM_017017683.2:c.53T>C | XP_016873172.1:p.Val18Ala | |
| XM_024448511.1:c.60T>C | XP_024304279.1:p.Gly20= | |
| XM_024448512.1:c.60T>C | XP_024304280.1:p.Gly20= | |
| XM_024448513.1:c.60T>C | XP_024304281.1:p.Gly20= | |
| XM_024448514.1:c.60T>C | XP_024304282.1:p.Gly20= | |
| XM_024448515.1:c.60T>C | XP_024304283.1:p.Gly20= | |
| NM_000019.4:c.330T>C MANE Select | NP_000010.1:p.Gly110= | |
| NM_001386677.1:c.330T>C | NP_001373606.1:p.Gly110= | |
| NM_001386678.1:c.120+2358T>C | NP_001373607.1:n.120+2358T>C | |
| NM_001386679.1:c.37+16T>C | NP_001373608.1:n.37+16T>C | |
| NM_001386681.1:c.60T>C | NP_001373610.1:p.Gly20= | |
| NM_001386682.1:c.60T>C | NP_001373611.1:p.Gly20= | |
| NM_001386685.1:c.60T>C | NP_001373614.1:p.Gly20= | |
| NM_001386686.1:c.60T>C | NP_001373615.1:p.Gly20= | |
| NM_001386687.1:c.60T>C | NP_001373616.1:p.Gly20= | |
| NM_001386688.1:c.60T>C | NP_001373617.1:p.Gly20= | |
| NM_001386689.1:c.60T>C | NP_001373618.1:p.Gly20= | |
| NM_001386690.1:c.60T>C | NP_001373619.1:p.Gly20= | |
| NM_001386691.1:c.60T>C | NP_001373620.1:p.Gly20= | |
| NR_170162.1:n.370T>C | ||
| NR_170163.1:n.464T>C |