Linked Data
MyVariant Identifiers:
chr11:g.86665888T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.86954846T>G , CM000673.2:g.86954846T>G | GRCh38 |
| NC_000011.9:g.86665888T>G , CM000673.1:g.86665888T>G | GRCh37 |
| NC_000011.8:g.86343536T>G | NCBI36 |
| NG_011752.1:g.5546A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000531380.2:c.240A>C MANE Select | ENSP00000434034.1:p.Thr80= | |
| ENST00000531380.1:c.240A>C | ENSP00000434034.1:p.Thr80= | |
| NM_012193.3:c.240A>C | NP_036325.2:p.Thr80= | |
| NM_012193.4:c.240A>C MANE Select | NP_036325.2:p.Thr80= |