Linked Data
ClinVar Variation Id:
2112382
ClinVar RCV Id:
RCV003034527
dbSNP Id:
rs1567964295
gnomAD v2:
18-21134952-A-G
gnomAD v4:
18-23554988-A-G
MyVariant Identifiers:
chr18:g.21134952_21134955delinsGAAG (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.23554988A>G , CM000680.2:g.23554988A>G | GRCh38 |
| NC_000018.9:g.21134952A>G , CM000680.1:g.21134952A>G | GRCh37 |
| NC_000018.8:g.19388950A>G | NCBI36 |
| NG_012795.1:g.36630T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000269228.10:c.1327-4T>C MANE Select | ENSP00000269228.4:n.1327-4T>C | |
| ENST00000269228.9:c.1327-4T>C | ENSP00000269228.4:n.1327-4T>C | |
| ENST00000540608.5:n.1241-4T>C | ||
| ENST00000591051.1:c.609-4T>C | ||
| NM_000271.4:c.1327-4T>C | NP_000262.2:n.1327-4T>C | |
| XM_005258277.1:c.1378-4T>C | XP_005258334.1:n.1378-4T>C | |
| XM_005258278.3:c.1378-4T>C | XP_005258335.1:n.1378-4T>C | |
| XM_005258279.1:c.1327-4T>C | XP_005258336.1:n.1327-4T>C | |
| XM_006722479.2:c.1378-4T>C | XP_006722542.1:n.1378-4T>C | |
| XM_011526015.1:c.913-4T>C | XP_011524317.1:n.913-4T>C | |
| XM_005258278.5:c.1378-4T>C | XP_005258335.1:n.1378-4T>C | |
| XM_005258279.2:c.1327-4T>C | XP_005258336.1:n.1327-4T>C | |
| XM_006722479.3:c.1378-4T>C | XP_006722542.1:n.1378-4T>C | |
| XM_017025784.1:c.1378-4T>C | XP_016881273.1:n.1378-4T>C | |
| XM_017025785.1:c.1378-4T>C | XP_016881274.1:n.1378-4T>C | |
| XM_017025786.1:c.1327-4T>C | XP_016881275.1:n.1327-4T>C | |
| XM_017025787.1:c.1327-4T>C | XP_016881276.1:n.1327-4T>C | |
| NM_000271.5:c.1327-4T>C MANE Select | NP_000262.2:n.1327-4T>C |