Linked Data
ClinVar Variation Id:
2947677
ClinVar RCV Id:
RCV003804307
gnomAD v4:
5-1293908-G-T
MyVariant Identifiers:
chr5:g.1294023G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1293908G>T , CM000667.2:g.1293908G>T | GRCh38 |
| NC_000005.9:g.1294023G>T , CM000667.1:g.1294023G>T | GRCh37 |
| NC_000005.8:g.1347023G>T | NCBI36 |
| NG_009265.1:g.6140C>A , LRG_343:g.6140C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310581.10:c.978C>A MANE Select | ENSP00000309572.5:p.Ala326= | |
| ENST00000656021.1:c.978C>A | ENSP00000499759.1:p.Ala326= | |
| ENST00000310581.9:c.978C>A | ENSP00000309572.5:p.Ala326= | |
| ENST00000334602.10:c.978C>A | ENSP00000334346.6:p.Ala326= | |
| ENST00000460137.6:c.978C>A | ENSP00000425003.1:p.Ala326= | |
| ENST00000508104.2:c.978C>A | ENSP00000426042.2:p.Ala326= | |
| NM_001193376.1:c.978C>A | NP_001180305.1:p.Ala326= | |
| NM_198253.2:c.978C>A , LRG_343t1:c.978C>A | NP_937983.2:p.Ala326= | |
| NR_149162.1:n.1036C>A | ||
| NR_149163.1:n.1036C>A | ||
| NM_001193376.2:c.978C>A | NP_001180305.1:p.Ala326= | |
| NM_198253.3:c.978C>A MANE Select | NP_937983.2:p.Ala326= | |
| NR_149162.2:n.1057C>A | ||
| NR_149163.2:n.1057C>A | ||
| NM_001193376.3:c.978C>A | NP_001180305.1:p.Ala326= | |
| NR_149162.3:n.1057C>A | ||
| NR_149163.3:n.1057C>A |