Linked Data
ClinVar Variation Id:
2159155
ClinVar RCV Id:
RCV003072667
dbSNP Id:
rs775550642
gnomAD v2:
17-4802072-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4898777G>C , CM000679.2:g.4898777G>C | GRCh38 |
| NC_000017.10:g.4802072G>C , CM000679.1:g.4802072G>C | GRCh37 |
| NC_000017.9:g.4742851G>C | NCBI36 |
| NG_008029.2:g.9299C>G | |
| NG_028005.1:g.70438G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649488.2:c.1441C>G MANE Select | ENSP00000497829.1:p.Arg481Gly | |
| ENST00000649830.1:c.*77C>G | ENSP00000496907.1:n.*77C>G | |
| ENST00000652550.1:n.1167C>G | ||
| ENST00000293780.4:c.1441C>G | ENSP00000293780.4:p.Arg481Gly | |
| ENST00000572438.1:n.1127C>G | ||
| NM_000080.3:c.1441C>G | NP_000071.1:p.Arg481Gly | |
| NM_000080.4:c.1441C>G MANE Select | NP_000071.1:p.Arg481Gly | |
| XM_017024115.1:c.1405C>G | XP_016879604.1:p.Arg469Gly |