Linked Data
dbSNP Id:
rs755196965
ExAC:
2:73799919 C / G
gnomAD v2:
2-73799919-C-G
gnomAD v4:
2-73572792-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.73572792C>G , CM000664.2:g.73572792C>G | GRCh38 |
| NC_000002.11:g.73799919C>G , CM000664.1:g.73799919C>G | GRCh37 |
| NC_000002.10:g.73653427C>G | NCBI36 |
| NG_011690.1:g.192040C>G , LRG_741:g.192040C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682565.1:c.10534C>G | ENSP00000507671.1:p.Pro3512Ala | |
| ENST00000682801.1:c.10534C>G | ENSP00000507862.1:p.Pro3512Ala | |
| ENST00000682859.1:c.10534C>G | ENSP00000508222.1:p.Pro3512Ala | |
| ENST00000683791.1:c.3620C>G | ||
| ENST00000684460.1:c.7815C>G | ||
| ENST00000684548.1:c.10534C>G | ENSP00000507421.1:p.Pro3512Ala | |
| ENST00000684590.1:c.4981C>G | ENSP00000507376.1:p.Pro1661Ala | |
| ENST00000684656.1:c.7860C>G | ||
| ENST00000613296.6:c.10915C>G MANE Select | ENSP00000482968.1:p.Pro3639Ala | |
| ENST00000651057.1:c.1069C>G | ENSP00000498504.1:p.Pro357Ala | |
| ENST00000651434.1:c.2271C>G | ||
| ENST00000651750.1:c.303C>G | ||
| ENST00000652487.1:c.2012C>G | ||
| ENST00000423048.5:c.4406C>G | ENSP00000399833.1:n.4406C>G | |
| ENST00000484298.5:c.10789C>G | ENSP00000478155.1:p.Pro3597Ala | |
| ENST00000613296.4:c.10915C>G | ENSP00000482968.1:p.Pro3639Ala | |
| ENST00000614410.4:c.10915C>G | ENSP00000479094.1:p.Pro3639Ala | |
| ENST00000620466.4:n.4718C>G | ||
| NM_015120.4:c.10918C>G , LRG_741t1:c.10918C>G | NP_055935.4:p.Pro3640Ala | |
| NM_001378454.1:c.10915C>G MANE Select | NP_001365383.1:p.Pro3639Ala |