Linked Data
MyVariant Identifiers:
chr5:g.127597457T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128261765T>G , CM000667.2:g.128261765T>G | GRCh38 |
| NC_000005.9:g.127597457T>G , CM000667.1:g.127597457T>G | GRCh37 |
| NC_000005.8:g.127625356T>G | NCBI36 |
| NG_008750.1:g.281279A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262464.9:c.8335A>C MANE Select | ENSP00000262464.4:p.Arg2779= | |
| ENST00000262464.8:c.8335A>C | ENSP00000262464.4:p.Arg2779= | |
| ENST00000508053.5:c.8335A>C | ENSP00000424571.1:p.Arg2779= | |
| ENST00000619499.4:c.8332A>C | ENSP00000482132.1:p.Arg2778= | |
| NM_001999.3:c.8335A>C | NP_001990.2:p.Arg2779= | |
| XM_017009228.2:c.8182A>C | XP_016864717.1:p.Arg2728= | |
| NM_001999.4:c.8335A>C MANE Select | NP_001990.2:p.Arg2779= |