Linked Data
MyVariant Identifiers:
chr10:g.105797511G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.104037753G>A , CM000672.2:g.104037753G>A | GRCh38 |
| NC_000010.10:g.105797511G>A , CM000672.1:g.105797511G>A | GRCh37 |
| NC_000010.9:g.105787501G>A | NCBI36 |
| NG_007069.1:g.53128C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369733.8:c.2956C>T | ENSP00000358748.3:p.Leu986= | |
| ENST00000648076.2:c.3091C>T MANE Select | ENSP00000497653.1:p.Leu1031= | |
| ENST00000353479.9:c.3091C>T | ENSP00000340937.5:p.Leu1031= | |
| ENST00000369733.7:c.2956C>T | ENSP00000358748.3:p.Leu986= | |
| NM_000494.3:c.3091C>T | NP_000485.3:p.Leu1031= | |
| NM_000494.4:c.3091C>T MANE Select | NP_000485.3:p.Leu1031= |