Linked Data
ClinVar Variation Id:
1161555
ClinVar RCV Id:
RCV001506108
dbSNP Id:
rs1953579486
gnomAD v4:
11-17387378-G-A
MyVariant Identifiers:
chr11:g.17408925G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17387378G>A , CM000673.2:g.17387378G>A | GRCh38 |
| NC_000011.9:g.17408925G>A , CM000673.1:g.17408925G>A | GRCh37 |
| NC_000011.8:g.17365501G>A | NCBI36 |
| NG_012446.1:g.6282C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682350.1:c.453C>T | ENSP00000508090.1:p.Ile151= | |
| ENST00000682764.1:c.453C>T | ENSP00000506780.1:p.Ile151= | |
| ENST00000339994.5:c.714C>T MANE Select | ENSP00000345708.4:p.Ile238= | |
| ENST00000339994.4:c.714C>T | ENSP00000345708.4:p.Ile238= | |
| ENST00000526912.1:c.453C>T | ENSP00000432729.1:p.Ile151= | |
| ENST00000528731.1:c.453C>T | ENSP00000434755.1:p.Ile151= | |
| NM_000525.3:c.714C>T | NP_000516.3:p.Ile238= | |
| NM_001166290.1:c.453C>T | NP_001159762.1:p.Ile151= | |
| XM_006718226.2:c.453C>T | XP_006718289.1:p.Ile151= | |
| XR_930867.1:n.872C>T | ||
| XM_006718226.3:c.453C>T | XP_006718289.1:p.Ile151= | |
| XM_017017680.1:c.453C>T | XP_016873169.1:p.Ile151= | |
| NM_001166290.2:c.453C>T | NP_001159762.1:p.Ile151= | |
| NM_001377296.1:c.453C>T | NP_001364225.1:p.Ile151= | |
| NM_001377297.1:c.453C>T | NP_001364226.1:p.Ile151= | |
| NM_000525.4:c.714C>T MANE Select | NP_000516.3:p.Ile238= |