Linked Data
gnomAD v4:
2-208129661-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.208129661G>A , CM000664.2:g.208129661G>A | GRCh38 |
| NC_000002.11:g.208994385G>A , CM000664.1:g.208994385G>A | GRCh37 |
| NC_000002.10:g.208702630G>A | NCBI36 |
| NG_008038.1:g.5170C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282141.4:c.32C>T MANE Select | ENSP00000282141.3:p.Ala11Val | |
| ENST00000282141.3:c.32C>T | ENSP00000282141.3:p.Ala11Val | |
| NM_020989.3:c.32C>T | NP_066269.1:p.Ala11Val | |
| NR_038437.1:n.98-7395G>A | ||
| XM_011510661.1:c.32C>T | XP_011508963.1:p.Ala11Val | |
| XM_011510662.1:c.32C>T | XP_011508964.1:p.Ala11Val | |
| XM_011510663.1:c.-98C>T | XP_011508965.1:n.-98C>T | |
| NM_020989.4:c.32C>T MANE Select | NP_066269.1:p.Ala11Val |