Linked Data
ClinVar Variation Id:
761081
ClinVar RCV Id:
RCV000939090
dbSNP Id:
rs1580412048
MyVariant Identifiers:
chr5:g.54529064C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.55233236C>T , CM000667.2:g.55233236C>T | GRCh38 |
| NC_000005.9:g.54529064C>T , CM000667.1:g.54529064C>T | GRCh37 |
| NC_000005.8:g.54564821C>T | NCBI36 |
| NG_034201.1:g.5482G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282572.5:c.288G>A MANE Select | ENSP00000282572.4:p.Gln96= | |
| ENST00000282572.4:c.288G>A | ENSP00000282572.4:p.Gln96= | |
| ENST00000501463.2:c.288G>A | ENSP00000422485.1:p.Gln96= | |
| NM_021147.4:c.288G>A | NP_066970.3:p.Gln96= | |
| NR_125346.1:n.482G>A | ||
| NR_125347.1:n.482G>A | ||
| NM_021147.5:c.288G>A MANE Select | NP_066970.3:p.Gln96= | |
| NR_125346.2:n.373G>A | ||
| NR_125347.2:n.373G>A |