Linked Data
ClinVar Variation Id:
2288420
ClinVar RCV Id:
RCV002864336
dbSNP Id:
rs1806122530
gnomAD v4:
8-54627989-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.54627989G>C , CM000670.2:g.54627989G>C | GRCh38 |
| NC_000008.10:g.55540549G>C , CM000670.1:g.55540549G>C | GRCh37 |
| NC_000008.9:g.55703102G>C | NCBI36 |
| NG_009840.1:g.16923G>C | |
| NG_009840.2:g.16923G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000220676.2:c.4107G>C MANE Select | ENSP00000220676.1:p.Gln1369His | |
| ENST00000636932.1:c.787+5701G>C | ENSP00000489857.1:n.787+5701G>C | |
| ENST00000637698.1:c.787+5701G>C | ENSP00000490104.1:n.787+5701G>C | |
| ENST00000220676.1:c.4107G>C | ENSP00000220676.1:p.Gln1369His | |
| NM_006269.1:c.4107G>C | NP_006260.1:p.Gln1369His | |
| XM_017013721.1:c.4128G>C | XP_016869210.1:p.Gln1376His | |
| XM_017013722.1:c.4107G>C | XP_016869211.1:p.Gln1369His | |
| NM_001375654.1:c.787+5701G>C | NP_001362583.1:n.787+5701G>C | |
| NM_006269.2:c.4107G>C MANE Select | NP_006260.1:p.Gln1369His |