Linked Data
ClinVar Variation Id:
647843
ClinVar RCV Id:
RCV000802446
dbSNP Id:
rs1580553882
MyVariant Identifiers:
chr5:g.79970947G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.80675128G>A , CM000667.2:g.80675128G>A | GRCh38 |
| NC_000005.9:g.79970947G>A , CM000667.1:g.79970947G>A | GRCh37 |
| NC_000005.8:g.80006703G>A | NCBI36 |
| NG_016607.1:g.25654G>A | |
| NG_016607.2:g.25654G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265081.7:c.1173G>A MANE Select | ENSP00000265081.6:p.Val391= | |
| ENST00000658259.1:c.1005G>A | ENSP00000499617.1:p.Val335= | |
| ENST00000667069.1:c.1173G>A | ENSP00000499502.1:p.Val391= | |
| ENST00000670357.1:c.1173G>A | ENSP00000499791.1:p.Val391= | |
| ENST00000265081.6:c.1173G>A | ENSP00000265081.6:p.Val391= | |
| NM_002439.4:c.1173G>A | NP_002430.3:p.Val391= | |
| NM_002439.5:c.1173G>A MANE Select | NP_002430.3:p.Val391= |