Linked Data
MyVariant Identifiers:
chr11:g.6340690T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6319460T>A , CM000673.2:g.6319460T>A | GRCh38 |
| NC_000011.9:g.6340690T>A , CM000673.1:g.6340690T>A | GRCh37 |
| NC_000011.8:g.6297266T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.489A>T MANE Select | ENSP00000307292.3:p.Gly163= | |
| ENST00000303927.3:c.489A>T | ENSP00000307292.3:p.Gly163= | |
| ENST00000524852.1:n.275A>T | ||
| ENST00000530979.1:c.585A>T | ENSP00000432047.1:p.Gly195= | |
| ENST00000532354.1:n.511A>T | ||
| NM_145040.2:c.489A>T | NP_659477.2:p.Gly163= | |
| XR_930997.1:n.720+1240T>A | ||
| XR_001748106.1:n.71T>A | ||
| XR_242848.4:n.320T>A | ||
| NM_145040.3:c.489A>T MANE Select | NP_659477.2:p.Gly163= |