Linked Data
MyVariant Identifiers:
chr5:g.127680102T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128344410T>C , CM000667.2:g.128344410T>C | GRCh38 |
| NC_000005.9:g.127680102T>C , CM000667.1:g.127680102T>C | GRCh37 |
| NC_000005.8:g.127708001T>C | NCBI36 |
| NG_008750.1:g.198634A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262464.9:c.3318A>G MANE Select | ENSP00000262464.4:p.Leu1106= | |
| ENST00000262464.8:c.3318A>G | ENSP00000262464.4:p.Leu1106= | |
| ENST00000508053.5:c.3318A>G | ENSP00000424571.1:p.Leu1106= | |
| ENST00000508989.5:c.3219A>G | ENSP00000425596.1:p.Leu1073= | |
| ENST00000619499.4:c.3315A>G | ENSP00000482132.1:p.Leu1105= | |
| NM_001999.3:c.3318A>G | NP_001990.2:p.Leu1106= | |
| XM_017009228.2:c.3165A>G | XP_016864717.1:p.Leu1055= | |
| NM_001999.4:c.3318A>G MANE Select | NP_001990.2:p.Leu1106= |