Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71124505T>C , CM000664.2:g.71124505T>C | GRCh38 |
| NC_000002.11:g.71351635T>C , CM000664.1:g.71351635T>C | GRCh37 |
| NC_000002.10:g.71205143T>C | NCBI36 |
| NG_008977.1:g.10760A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000244217.6:c.79A>G MANE Select | ENSP00000244217.5:p.Arg27Gly | |
| ENST00000244217.5:c.79A>G | ENSP00000244217.5:p.Arg27Gly | |
| ENST00000486135.1:c.-207A>G | ENSP00000441569.1:n.-207A>G | |
| ENST00000494660.6:c.-207A>G | ENSP00000437361.1:n.-207A>G | |
| NM_032601.3:c.79A>G | NP_115990.3:p.Arg27Gly | |
| XM_005264613.2:c.79A>G | XP_005264670.1:p.Arg27Gly | |
| XR_939729.1:n.148A>G | ||
| XR_939729.2:n.148A>G | ||
| NM_032601.4:c.79A>G MANE Select | NP_115990.3:p.Arg27Gly |