Linked Data
ClinVar Variation Id:
337081
ClinVar RCV Id:
RCV000278941
RCV000336449
RCV000555724
RCV000517874
RCV000997172
RCV002446597
RCV003418060
dbSNP Id:
rs754780894
ExAC:
2:74594210 T / C
gnomAD v2:
2-74594210-T-C
gnomAD v3:
2-74367083-T-C
gnomAD v4:
2-74367083-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.74367083T>C , CM000664.2:g.74367083T>C | GRCh38 |
| NC_000002.11:g.74594210T>C , CM000664.1:g.74594210T>C | GRCh37 |
| NC_000002.10:g.74447718T>C | NCBI36 |
| NG_008735.2:g.30005A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361874.8:c.2278A>G | ENSP00000354791.4:p.Met760Val | |
| ENST00000628224.3:c.2278A>G MANE Select | ENSP00000487279.2:p.Met760Val | |
| ENST00000680606.1:c.2227A>G | ENSP00000505612.1:p.Met743Val | |
| ENST00000361874.7:c.2278A>G | ENSP00000354791.3:p.Met760Val | |
| ENST00000394003.7:c.2257A>G | ENSP00000377571.3:p.Met753Val | |
| ENST00000409240.5:c.2167A>G | ENSP00000386406.1:p.Met723Val | |
| ENST00000409438.5:c.1876A>G | ENSP00000387270.1:p.Met626Val | |
| ENST00000409567.7:c.2218A>G | ENSP00000386843.3:p.Met740Val | |
| ENST00000409868.5:c.2227A>G | ENSP00000387327.1:p.Met743Val | |
| ENST00000434055.5:c.2167A>G | ENSP00000416711.1:p.Met723Val | |
| ENST00000466110.5:n.3095A>G | ||
| ENST00000495643.1:n.306A>G | ||
| ENST00000497666.1:n.96+2217A>G | ||
| ENST00000628224.2:c.2227A>G | ENSP00000487279.1:p.Met743Val | |
| ENST00000633691.1:c.1876A>G | ENSP00000487724.1:p.Met626Val | |
| NM_001135040.2:c.2218A>G | NP_001128512.1:p.Met740Val | |
| NM_001135041.2:c.1876A>G | NP_001128513.1:p.Met626Val | |
| NM_001190836.1:c.2167A>G | NP_001177765.1:p.Met723Val | |
| NM_001190837.1:c.2257A>G | NP_001177766.1:p.Met753Val | |
| NM_004082.4:c.2278A>G | NP_004073.2:p.Met760Val | |
| NM_023019.3:c.1876A>G | NP_075408.1:p.Met626Val | |
| NR_033935.1:n.2479A>G | ||
| NM_001135040.3:c.2218A>G | NP_001128512.1:p.Met740Val | |
| NM_001135041.3:c.1876A>G | NP_001128513.1:p.Met626Val | |
| NM_001190836.2:c.2167A>G | NP_001177765.1:p.Met723Val | |
| NM_001190837.2:c.2257A>G | NP_001177766.1:p.Met753Val | |
| NM_001378991.1:c.2227A>G | NP_001365920.1:p.Met743Val | |
| NM_001378992.1:c.2209A>G | NP_001365921.1:p.Met737Val | |
| NM_004082.5:c.2278A>G MANE Select | NP_004073.2:p.Met760Val | |
| NM_023019.4:c.1876A>G | NP_075408.1:p.Met626Val | |
| NR_033935.2:n.2258A>G |