Linked Data
MyVariant Identifiers:
chr5:g.139494195C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.140114610C>G , CM000667.2:g.140114610C>G | GRCh38 |
| NC_000005.9:g.139494195C>G , CM000667.1:g.139494195C>G | GRCh37 |
| NC_000005.8:g.139474379C>G | NCBI36 |
| NG_041813.1:g.5488C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331327.5:c.429C>G MANE Select | ENSP00000332706.3:p.Leu143= | |
| ENST00000651386.1:c.429C>G | ENSP00000499133.1:p.Leu143= | |
| ENST00000331327.4:c.429C>G | ENSP00000332706.3:p.Leu143= | |
| NM_005859.4:c.429C>G | NP_005850.1:p.Leu143= | |
| NM_005859.5:c.429C>G MANE Select | NP_005850.1:p.Leu143= |