Linked Data
ClinVar Variation Id:
1983785
ClinVar RCV Id:
RCV002756661
dbSNP Id:
rs1811939577
gnomAD v4:
8-43122446-C-T
MyVariant Identifiers:
chr8:g.42977589C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.43122446C>T , CM000670.2:g.43122446C>T | GRCh38 |
| NC_000008.10:g.42977589C>T , CM000670.1:g.42977589C>T | GRCh37 |
| NC_000008.9:g.43096746C>T | NCBI36 |
| NG_033235.1:g.33941C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331373.10:c.622C>T MANE Select | ENSP00000331258.5:p.Leu208= | |
| ENST00000614426.2:c.*418C>T | ENSP00000478821.2:n.*418C>T | |
| ENST00000674646.1:c.340C>T | ENSP00000501703.1:p.Leu114= | |
| ENST00000674676.1:c.340C>T | ENSP00000502544.1:p.Leu114= | |
| ENST00000674782.1:c.*542C>T | ENSP00000501683.1:n.*542C>T | |
| ENST00000674937.1:c.580C>T | ENSP00000501823.1:p.Leu194= | |
| ENST00000675322.1:c.340C>T | ENSP00000502235.1:p.Leu114= | |
| ENST00000675675.1:c.340C>T | ENSP00000501793.1:p.Leu114= | |
| ENST00000676178.1:c.*407C>T | ENSP00000502007.1:n.*407C>T | |
| ENST00000676193.1:c.622C>T | ENSP00000502774.1:p.Leu208= | |
| ENST00000331373.9:c.622C>T | ENSP00000331258.5:p.Leu208= | |
| ENST00000614426.1:c.622C>T | ENSP00000478821.1:p.Leu208= | |
| NM_001277971.1:c.622C>T | NP_001264900.1:p.Leu208= | |
| NM_032237.4:c.622C>T | NP_115613.1:p.Leu208= | |
| XM_011544668.1:c.622C>T | XP_011542970.1:p.Leu208= | |
| XM_011544669.1:c.622C>T | XP_011542971.1:p.Leu208= | |
| NM_032237.5:c.622C>T MANE Select | NP_115613.1:p.Leu208= | |
| NM_001277971.2:c.622C>T | NP_001264900.1:p.Leu208= |