Linked Data
gnomAD v4:
11-118168718-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118168718G>A , CM000673.2:g.118168718G>A | GRCh38 |
| NC_000011.9:g.118039433G>A , CM000673.1:g.118039433G>A | GRCh37 |
| NC_000011.8:g.117544643G>A | NCBI36 |
| NG_042217.1:g.12905C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000278947.6:c.104C>T MANE Select | ENSP00000278947.5:p.Pro35Leu | |
| ENST00000658882.1:c.208C>T | ENSP00000499572.1:p.Leu70= | |
| ENST00000665446.1:n.340C>T | ||
| ENST00000669850.1:n.346C>T | ||
| ENST00000278947.5:c.104C>T | ENSP00000278947.5:p.Pro35Leu | |
| NM_004588.4:c.104C>T | NP_004579.1:p.Pro35Leu | |
| NM_004588.5:c.104C>T MANE Select | NP_004579.1:p.Pro35Leu |