Linked Data
MyVariant Identifiers:
chr5:g.71015183T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.71719356T>G , CM000667.2:g.71719356T>G | GRCh38 |
| NC_000005.9:g.71015183T>G , CM000667.1:g.71015183T>G | GRCh37 |
| NC_000005.8:g.71050939T>G | NCBI36 |
| NG_015988.1:g.5194T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296777.5:c.63T>G MANE Select | ENSP00000296777.4:p.Pro21= | |
| ENST00000296777.4:c.63T>G | ENSP00000296777.4:p.Pro21= | |
| NM_004291.3:c.63T>G | NP_004282.1:p.Pro21= | |
| NM_004291.4:c.63T>G MANE Select | NP_004282.1:p.Pro21= |