Linked Data
gnomAD v4:
2-38075039-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38075039C>G , CM000664.2:g.38075039C>G | GRCh38 |
| NC_000002.11:g.38302182C>G , CM000664.1:g.38302182C>G | GRCh37 |
| NC_000002.10:g.38155686C>G | NCBI36 |
| NG_008386.2:g.6063G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000490576.2:c.350G>C | ENSP00000478839.2:p.Arg117Pro | |
| ENST00000610745.5:c.350G>C MANE Select | ENSP00000478561.1:p.Arg117Pro | |
| ENST00000490576.1:c.350G>C | ENSP00000478839.1:p.Arg117Pro | |
| ENST00000494864.1:c.-70-3729G>C | ENSP00000479876.1:n.-70-3729G>C | |
| ENST00000610745.4:c.350G>C | ENSP00000478561.1:p.Arg117Pro | |
| ENST00000613082.1:n.376-631G>C | ||
| ENST00000614273.1:c.350G>C | ENSP00000483678.1:p.Arg117Pro | |
| NM_000104.3:c.350G>C | NP_000095.2:p.Arg117Pro | |
| NM_000104.4:c.350G>C MANE Select | NP_000095.2:p.Arg117Pro |