Linked Data
MyVariant Identifiers:
chr11:g.59211199A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.59443726A>G , CM000673.2:g.59443726A>G | GRCh38 |
| NC_000011.9:g.59211199A>G , CM000673.1:g.59211199A>G | GRCh37 |
| NC_000011.8:g.58967775A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000641045.1:c.558A>G MANE Select | ENSP00000493195.1:p.Pro186= | |
| ENST00000302030.2:c.558A>G | ENSP00000303096.2:p.Pro186= | |
| NM_001004728.1:c.558A>G | NP_001004728.1:p.Pro186= | |
| XM_011544810.1:c.558A>G | XP_011543112.1:p.Pro186= | |
| NM_001004728.2:c.558A>G MANE Select | NP_001004728.1:p.Pro186= |