Linked Data
dbSNP Id:
rs111983852
ExAC:
20:60503273 G / C
gnomAD v2:
20-60503273-G-C
gnomAD v3:
20-61928215-G-C
gnomAD v4:
20-61928215-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.61928215G>C , CM000682.2:g.61928215G>C | GRCh38 |
| NC_000020.10:g.60503273G>C , CM000682.1:g.60503273G>C | GRCh37 |
| NC_000020.9:g.59936668G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614565.5:c.1797G>C MANE Select | ENSP00000484928.1:p.Gly599= | |
| ENST00000543233.2:c.1575G>C | ENSP00000443301.1:p.Gly525= | |
| ENST00000611855.4:c.1515G>C | ENSP00000480844.1:p.Gly505= | |
| ENST00000614565.4:c.1797G>C | ENSP00000484928.1:p.Gly599= | |
| NM_001252338.2:c.1686G>C | NP_001239267.1:p.Gly562= | |
| NM_001252339.2:c.1575G>C | NP_001239268.1:p.Gly525= | |
| NM_001794.4:c.1797G>C | NP_001785.2:p.Gly599= | |
| NM_001794.5:c.1797G>C MANE Select | NP_001785.2:p.Gly599= | |
| NM_001252339.3:c.1575G>C | NP_001239268.1:p.Gly525= |