Linked Data
MyVariant Identifiers:
chr11:g.17575006A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17553459A>C , CM000673.2:g.17553459A>C | GRCh38 |
| NC_000011.9:g.17575006A>C , CM000673.1:g.17575006A>C | GRCh37 |
| NC_000011.8:g.17531582A>C | NCBI36 |
| NG_033191.1:g.11087A>C | |
| NG_033191.2:g.11087A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399391.7:c.516A>C | ENSP00000382323.2:p.Gly172= | |
| ENST00000399397.6:c.480A>C MANE Select | ENSP00000382329.2:p.Gly160= | |
| ENST00000399391.6:c.516A>C | ENSP00000382323.2:p.Gly172= | |
| ENST00000399397.5:c.480A>C | ENSP00000382329.2:p.Gly160= | |
| ENST00000498332.5:n.386A>C | ||
| NM_001277269.1:c.516A>C | NP_001264198.1:p.Gly172= | |
| NM_001292063.1:c.480A>C | NP_001278992.1:p.Gly160= | |
| NM_001277269.2:c.516A>C | NP_001264198.1:p.Gly172= | |
| NM_001292063.2:c.480A>C MANE Select | NP_001278992.1:p.Gly160= |