Linked Data
ClinVar Variation Id:
166650
dbSNP Id:
rs727503796
gnomAD v2:
11-108012428-G-T
gnomAD v3:
11-108141701-G-T
gnomAD v4:
11-108141701-G-T
PubMed:
PMID:1346617
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108141701G>T , CM000673.2:g.108141701G>T | GRCh38 |
| NC_000011.9:g.108012428G>T , CM000673.1:g.108012428G>T | GRCh37 |
| NC_000011.8:g.107517638G>T | NCBI36 |
| NG_009888.1:g.25171G>T | |
| NG_009888.2:g.29997G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265838.9:c.826+1G>T MANE Select | ENSP00000265838.4:n.826+1G>T | |
| ENST00000671707.1:n.921+1G>T | ||
| ENST00000672031.1:c.826+1G>T | ENSP00000500463.1:n.826+1G>T | |
| ENST00000672284.1:c.556+1G>T | ENSP00000500444.1:n.556+1G>T | |
| ENST00000672354.1:c.826+1G>T | ENSP00000500490.1:n.826+1G>T | |
| ENST00000672367.1:c.463+1G>T | ENSP00000500209.1:n.463+1G>T | |
| ENST00000672580.1:c.*81+1G>T | ENSP00000500366.1:n.*81+1G>T | |
| ENST00000672907.1:c.511+1G>T | ENSP00000500928.1:n.511+1G>T | |
| ENST00000673000.1:n.914+1G>T | ||
| ENST00000673531.1:c.556+1G>T | ENSP00000500163.1:n.556+1G>T | |
| ENST00000265838.8:c.826+1G>T | ENSP00000265838.4:n.826+1G>T | |
| ENST00000531813.5:c.*299+1G>T | ENSP00000435965.1:n.*299+1G>T | |
| ENST00000532792.5:n.321+1G>T | ||
| ENST00000533610.1:n.287+1G>T | ||
| NM_000019.3:c.826+1G>T | NP_000010.1:n.826+1G>T | |
| XM_006718834.2:c.556+1G>T | XP_006718897.1:n.556+1G>T | |
| XM_006718835.2:c.556+1G>T | XP_006718898.1:n.556+1G>T | |
| XM_006718835.3:c.556+1G>T | XP_006718898.1:n.556+1G>T | |
| XM_017017681.1:c.556+1G>T | XP_016873170.1:n.556+1G>T | |
| XM_017017682.2:c.448+1G>T | XP_016873171.1:n.448+1G>T | |
| XM_017017683.2:c.448+1G>T | XP_016873172.1:n.448+1G>T | |
| XM_024448511.1:c.556+1G>T | XP_024304279.1:n.556+1G>T | |
| XM_024448512.1:c.556+1G>T | XP_024304280.1:n.556+1G>T | |
| XM_024448513.1:c.556+1G>T | XP_024304281.1:n.556+1G>T | |
| XM_024448514.1:c.556+1G>T | XP_024304282.1:n.556+1G>T | |
| XM_024448515.1:c.556+1G>T | XP_024304283.1:n.556+1G>T | |
| NM_000019.4:c.826+1G>T MANE Select | NP_000010.1:n.826+1G>T | |
| NM_001386677.1:c.826+1G>T | NP_001373606.1:n.826+1G>T | |
| NM_001386678.1:c.511+1G>T | NP_001373607.1:n.511+1G>T | |
| NM_001386679.1:c.529+1G>T | NP_001373608.1:n.529+1G>T | |
| NM_001386681.1:c.556+1G>T | NP_001373610.1:n.556+1G>T | |
| NM_001386682.1:c.556+1G>T | NP_001373611.1:n.556+1G>T | |
| NM_001386685.1:c.556+1G>T | NP_001373614.1:n.556+1G>T | |
| NM_001386686.1:c.556+1G>T | NP_001373615.1:n.556+1G>T | |
| NM_001386687.1:c.556+1G>T | NP_001373616.1:n.556+1G>T | |
| NM_001386688.1:c.556+1G>T | NP_001373617.1:n.556+1G>T | |
| NM_001386689.1:c.556+1G>T | NP_001373618.1:n.556+1G>T | |
| NM_001386690.1:c.556+1G>T | NP_001373619.1:n.556+1G>T | |
| NM_001386691.1:c.556+1G>T | NP_001373620.1:n.556+1G>T | |
| NR_170162.1:n.866+1G>T | ||
| NR_170163.1:n.859+1G>T |