Linked Data
MyVariant Identifiers:
chr11:g.70052261C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.70206155C>G , CM000673.2:g.70206155C>G | GRCh38 |
| NC_000011.9:g.70052261C>G , CM000673.1:g.70052261C>G | GRCh37 |
| NC_000011.8:g.69729909C>G | NCBI36 |
| NG_027966.1:g.7993C>G , LRG_228:g.7993C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301838.5:c.309C>G MANE Select | ENSP00000301838.5:p.Val103= | |
| ENST00000301838.4:c.309C>G | ENSP00000301838.4:p.Val103= | |
| NM_003824.3:c.309C>G , LRG_228t1:c.309C>G | NP_003815.1:p.Val103= | |
| NM_003824.4:c.309C>G MANE Select | NP_003815.1:p.Val103= |