Linked Data
ClinVar Variation Id:
14760
ClinVar RCV Id:
RCV000015882
dbSNP Id:
rs121912438
gnomAD v2:
21-33039612-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31667299G>C , CM000683.2:g.31667299G>C | GRCh38 |
| NC_000021.8:g.33039612G>C , CM000683.1:g.33039612G>C | GRCh37 |
| NC_000021.7:g.31961483G>C | NCBI36 |
| NG_008689.1:g.12678G>C , LRG_652:g.12678G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270142.11:c.281G>C MANE Select | ENSP00000270142.7:p.Gly94Ala | |
| ENST00000270142.10:c.281G>C | ENSP00000270142.6:p.Gly94Ala | |
| ENST00000389995.4:c.224G>C | ENSP00000374645.4:p.Gly75Ala | |
| ENST00000470944.1:n.1209G>C | ||
| ENST00000476106.5:n.544G>C | ||
| NM_000454.4:c.281G>C , LRG_652t1:c.281G>C | NP_000445.1:p.Gly94Ala | |
| NM_000454.5:c.281G>C MANE Select | NP_000445.1:p.Gly94Ala |