Linked Data
dbSNP Id:
rs757767396
ExAC:
12:6442600 A / G
gnomAD v2:
12-6442600-A-G
gnomAD v4:
12-6333434-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6333434A>G , CM000674.2:g.6333434A>G | GRCh38 |
| NC_000012.11:g.6442600A>G , CM000674.1:g.6442600A>G | GRCh37 |
| NC_000012.10:g.6312861A>G | NCBI36 |
| NG_007506.1:g.13662T>C , LRG_193:g.13662T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366159.9:n.439T>C | ||
| ENST00000437813.8:c.405T>C | ENSP00000513672.1:p.Tyr135= | |
| ENST00000440083.7:c.405T>C | ENSP00000413224.3:p.Tyr135= | |
| ENST00000535958.2:c.*232T>C | ENSP00000513673.1:n.*232T>C | |
| ENST00000698339.1:c.405T>C | ENSP00000513670.1:p.Tyr135= | |
| ENST00000698340.1:c.405T>C | ENSP00000513671.1:p.Tyr135= | |
| ENST00000162749.7:c.405T>C MANE Select | ENSP00000162749.2:p.Tyr135= | |
| ENST00000162749.6:c.405T>C | ENSP00000162749.2:p.Tyr135= | |
| ENST00000366159.8:c.405T>C | ENSP00000380389.3:p.Tyr135= | |
| ENST00000437813.7:n.366T>C | ||
| ENST00000440083.6:c.405T>C | ENSP00000413224.2:p.Tyr135= | |
| ENST00000534885.5:c.251T>C | ENSP00000441803.1:p.Ile84Thr | |
| ENST00000537842.5:n.9T>C | ||
| ENST00000539372.5:c.405T>C | ENSP00000442059.1:p.Tyr135= | |
| ENST00000540022.5:c.276T>C | ENSP00000438343.1:p.Tyr92= | |
| ENST00000543048.5:c.*16T>C | ENSP00000439981.1:n.*16T>C | |
| ENST00000543995.5:c.211T>C | ENSP00000442405.1:p.Leu71= | |
| NM_001065.3:c.405T>C , LRG_193t1:c.405T>C | NP_001056.1:p.Tyr135= | |
| NM_001346091.1:c.81T>C | NP_001333020.1:p.Tyr27= | |
| NM_001346092.1:c.-173T>C | NP_001333021.1:n.-173T>C | |
| NR_144351.1:n.708T>C | ||
| NM_001065.4:c.405T>C MANE Select | NP_001056.1:p.Tyr135= | |
| NM_001346091.2:c.81T>C | NP_001333020.1:p.Tyr27= | |
| NM_001346092.2:c.-173T>C | NP_001333021.1:n.-173T>C | |
| NR_144351.2:n.667T>C |