Linked Data
MyVariant Identifiers:
chr5:g.7520883G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.7520770G>C , CM000667.2:g.7520770G>C | GRCh38 |
| NC_000005.9:g.7520883G>C , CM000667.1:g.7520883G>C | GRCh37 |
| NC_000005.8:g.7573883G>C | NCBI36 |
| NG_046913.1:g.129541G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338316.9:c.441G>C MANE Select | ENSP00000342952.4:p.Val147= | |
| ENST00000338316.8:c.441G>C | ENSP00000342952.4:p.Val147= | |
| ENST00000484965.5:n.175G>C | ||
| ENST00000498598.1:n.140G>C | ||
| ENST00000537121.5:c.441G>C | ENSP00000444803.2:p.Val147= | |
| NM_020546.2:c.441G>C | NP_065433.2:p.Val147= | |
| XM_011513942.1:c.441G>C | XP_011512244.1:p.Val147= | |
| XR_427657.2:n.455G>C | ||
| XM_011513942.2:c.441G>C | XP_011512244.1:p.Val147= | |
| XR_001741973.1:n.455G>C | ||
| XR_001741974.2:n.455G>C | ||
| NM_020546.3:c.441G>C MANE Select | NP_065433.2:p.Val147= |