Linked Data
dbSNP Id:
rs779620286
ExAC:
11:22294515 G / C
gnomAD v2:
11-22294515-G-C
gnomAD v4:
11-22272969-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22272969G>C , CM000673.2:g.22272969G>C | GRCh38 |
| NC_000011.9:g.22294515G>C , CM000673.1:g.22294515G>C | GRCh37 |
| NC_000011.8:g.22251091G>C | NCBI36 |
| NG_015844.1:g.84794G>C , LRG_868:g.84794G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000532043.2:n.232G>C | ||
| ENST00000682266.1:c.1765G>C | ENSP00000507766.1:p.Val589Leu | |
| ENST00000682341.1:c.2173G>C | ENSP00000508251.1:p.Val725Leu | |
| ENST00000683197.1:c.2173G>C | ENSP00000507641.1:p.Val725Leu | |
| ENST00000683411.1:c.1765G>C | ENSP00000508397.1:p.Val589Leu | |
| ENST00000683437.1:c.1765G>C | ENSP00000508408.1:p.Val589Leu | |
| ENST00000683613.1:n.3209G>C | ||
| ENST00000684663.1:c.2170G>C | ENSP00000508009.1:p.Val724Leu | |
| ENST00000324559.9:c.2215G>C MANE Select | ENSP00000315371.9:p.Val739Leu | |
| ENST00000648804.1:n.2550G>C | ||
| ENST00000324559.8:c.2215G>C | ENSP00000315371.8:p.Val739Leu | |
| ENST00000532043.1:n.232G>C | ||
| NM_001142649.1:c.2212G>C | NP_001136121.1:p.Val738Leu | |
| NM_213599.2:c.2215G>C , LRG_868t1:c.2215G>C | NP_998764.1:p.Val739Leu | |
| XM_005252820.2:c.2173G>C | XP_005252877.2:p.Val725Leu | |
| XM_005252821.2:c.2170G>C | XP_005252878.2:p.Val724Leu | |
| XM_005252822.3:c.2137G>C | XP_005252879.1:p.Val713Leu | |
| XM_005252823.3:c.2134G>C | XP_005252880.1:p.Val712Leu | |
| XM_011519949.1:c.2122G>C | XP_011518251.1:p.Val708Leu | |
| XM_005252820.3:c.2173G>C | XP_005252877.2:p.Val725Leu | |
| XM_005252821.3:c.2170G>C | XP_005252878.2:p.Val724Leu | |
| XM_005252822.4:c.2137G>C | XP_005252879.1:p.Val713Leu | |
| XM_011519949.2:c.2122G>C | XP_011518251.1:p.Val708Leu | |
| NM_001142649.2:c.2212G>C | NP_001136121.1:p.Val738Leu | |
| NM_213599.3:c.2215G>C MANE Select | NP_998764.1:p.Val739Leu |