Linked Data
ClinVar Variation Id:
2024443
ClinVar RCV Id:
RCV002863323
gnomAD v4:
12-65170061-C-T
MyVariant Identifiers:
chr12:g.65563841C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65170061C>T , CM000674.2:g.65170061C>T | GRCh38 |
| NC_000012.11:g.65563841C>T , CM000674.1:g.65563841C>T | GRCh37 |
| NC_000012.10:g.63850108C>T | NCBI36 |
| NG_016210.1:g.5491C>T | |
| NG_016210.2:g.5491C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308330.3:c.465C>T MANE Select | ENSP00000308369.2:p.Gly155= | |
| ENST00000308330.2:c.465C>T | ENSP00000308369.2:p.Gly155= | |
| ENST00000541171.1:n.479C>T | ||
| NM_001167614.1:c.465C>T | NP_001161086.1:p.Gly155= | |
| NM_014319.4:c.465C>T | NP_055134.2:p.Gly155= | |
| NM_014319.5:c.465C>T MANE Select | NP_055134.2:p.Gly155= | |
| NM_001167614.2:c.465C>T | NP_001161086.1:p.Gly155= |