Linked Data
ClinVar Variation Id:
1613266
ClinVar RCV Id:
RCV002171186
dbSNP Id:
rs1291859932
gnomAD v4:
18-23560287-G-A
MyVariant Identifiers:
chr18:g.21140251G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.23560287G>A , CM000680.2:g.23560287G>A | GRCh38 |
| NC_000018.9:g.21140251G>A , CM000680.1:g.21140251G>A | GRCh37 |
| NC_000018.8:g.19394249G>A | NCBI36 |
| NG_012795.1:g.31331C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269228.10:c.825C>T MANE Select | ENSP00000269228.4:p.Thr275= | |
| ENST00000269228.9:c.825C>T | ENSP00000269228.4:p.Thr275= | |
| ENST00000540608.5:n.739C>T | ||
| ENST00000591051.1:c.56C>T | ||
| NM_000271.4:c.825C>T | NP_000262.2:p.Thr275= | |
| XM_005258277.1:c.825C>T | XP_005258334.1:p.Thr275= | |
| XM_005258278.3:c.825C>T | XP_005258335.1:p.Thr275= | |
| XM_005258279.1:c.825C>T | XP_005258336.1:p.Thr275= | |
| XM_006722479.2:c.825C>T | XP_006722542.1:p.Thr275= | |
| XM_011526015.1:c.360C>T | XP_011524317.1:p.Thr120= | |
| XM_005258278.5:c.825C>T | XP_005258335.1:p.Thr275= | |
| XM_005258279.2:c.825C>T | XP_005258336.1:p.Thr275= | |
| XM_006722479.3:c.825C>T | XP_006722542.1:p.Thr275= | |
| XM_017025784.1:c.825C>T | XP_016881273.1:p.Thr275= | |
| XM_017025785.1:c.825C>T | XP_016881274.1:p.Thr275= | |
| XM_017025786.1:c.825C>T | XP_016881275.1:p.Thr275= | |
| XM_017025787.1:c.825C>T | XP_016881276.1:p.Thr275= | |
| NM_000271.5:c.825C>T MANE Select | NP_000262.2:p.Thr275= |