Linked Data
dbSNP Id:
rs2101085992
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115732927T>G , CM000663.2:g.115732927T>G | GRCh38 |
| NC_000001.10:g.116275548T>G , CM000663.1:g.116275548T>G | GRCh37 |
| NC_000001.9:g.116077071T>G | NCBI36 |
| NG_008802.1:g.40879A>C , LRG_404:g.40879A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000488931.2:c.304A>C | ENSP00000518226.1:p.Lys102Gln | |
| ENST00000261448.6:c.580A>C MANE Select | ENSP00000261448.5:p.Lys194Gln | |
| ENST00000261448.5:c.580A>C | ENSP00000261448.5:p.Lys194Gln | |
| ENST00000488931.1:n.1A>C | ||
| NM_001232.3:c.580A>C , LRG_404t1:c.580A>C | NP_001223.2:p.Lys194Gln | |
| NM_001232.4:c.580A>C MANE Select | NP_001223.2:p.Lys194Gln |