Linked Data
gnomAD v3:
18-52906237-C-T
gnomAD v4:
18-52906237-C-T
MyVariant Identifiers:
chr18:g.50432607C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.52906237C>T , CM000680.2:g.52906237C>T | GRCh38 |
| NC_000018.9:g.50432607C>T , CM000680.1:g.50432607C>T | GRCh37 |
| NC_000018.8:g.48686605C>T | NCBI36 |
| NG_013341.1:g.571066C>T | |
| NG_013341.2:g.571066C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442544.7:c.606C>T MANE Select | ENSP00000389140.2:p.Leu202= | |
| ENST00000304775.12:c.407C>T | ||
| ENST00000412726.5:c.537C>T | ENSP00000397322.2:p.Leu179= | |
| ENST00000442544.6:c.606C>T | ENSP00000389140.2:p.Leu202= | |
| ENST00000579349.1:c.527C>T | ||
| ENST00000580024.1:n.519C>T | ||
| ENST00000581559.1:c.527C>T | ENSP00000463463.1:n.527C>T | |
| NM_005215.3:c.606C>T | NP_005206.2:p.Leu202= | |
| XM_011525843.1:c.606C>T | XP_011524145.1:p.Leu202= | |
| XM_011525845.1:c.606C>T | XP_011524147.1:p.Leu202= | |
| XM_011525846.1:c.606C>T | XP_011524148.1:p.Leu202= | |
| XM_017025568.1:c.606C>T | XP_016881057.1:p.Leu202= | |
| XM_017025569.1:c.606C>T | XP_016881058.1:p.Leu202= | |
| NM_005215.4:c.606C>T MANE Select | NP_005206.2:p.Leu202= |