Linked Data
ClinVar Variation Id:
331203
dbSNP Id:
rs377102890
ExAC:
2:136575222 C / A
gnomAD v2:
2-136575222-C-A
gnomAD v3:
2-135817652-C-A
gnomAD v4:
2-135817652-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.135817652C>A , CM000664.2:g.135817652C>A | GRCh38 |
| NC_000002.11:g.136575222C>A , CM000664.1:g.136575222C>A | GRCh37 |
| NC_000002.10:g.136291692C>A | NCBI36 |
| NG_008104.2:g.42518G>T , LRG_338:g.42518G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264162.7:c.1396G>T MANE Select | ENSP00000264162.2:p.Gly466Trp | |
| ENST00000264162.6:c.1396G>T | ENSP00000264162.2:p.Gly466Trp | |
| NM_002299.2:c.1396G>T , LRG_338t1:c.1396G>T | NP_002290.2:p.Gly466Trp | |
| NM_002299.3:c.1396G>T | NP_002290.2:p.Gly466Trp | |
| XM_017004088.2:c.1396G>T | XP_016859577.1:p.Gly466Trp | |
| NM_002299.4:c.1396G>T MANE Select | NP_002290.2:p.Gly466Trp |