Linked Data
ClinVar Variation Id:
2031439
ClinVar RCV Id:
RCV002898841
MyVariant Identifiers:
chr2:g.241808715C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869298C>T , CM000664.2:g.240869298C>T | GRCh38 |
| NC_000002.11:g.241808715C>T , CM000664.1:g.241808715C>T | GRCh37 |
| NC_000002.10:g.241457388C>T | NCBI36 |
| NG_008005.1:g.5554C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.294C>T MANE Select | ENSP00000302620.3:p.Asp98= | |
| ENST00000307503.3:c.294C>T | ENSP00000302620.3:p.Asp98= | |
| ENST00000472436.1:n.314C>T | ||
| NM_000030.2:c.294C>T | NP_000021.1:p.Asp98= | |
| XR_924060.1:n.405+935G>A | ||
| NM_000030.3:c.294C>T MANE Select | NP_000021.1:p.Asp98= |