Linked Data
MyVariant Identifiers:
chr10:g.105797476A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.104037718A>T , CM000672.2:g.104037718A>T | GRCh38 |
| NC_000010.10:g.105797476A>T , CM000672.1:g.105797476A>T | GRCh37 |
| NC_000010.9:g.105787466A>T | NCBI36 |
| NG_007069.1:g.53163T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369733.8:c.2991T>A | ENSP00000358748.3:p.Gly997= | |
| ENST00000648076.2:c.3126T>A MANE Select | ENSP00000497653.1:p.Gly1042= | |
| ENST00000353479.9:c.3126T>A | ENSP00000340937.5:p.Gly1042= | |
| ENST00000369733.7:c.2991T>A | ENSP00000358748.3:p.Gly997= | |
| NM_000494.3:c.3126T>A | NP_000485.3:p.Gly1042= | |
| NM_000494.4:c.3126T>A MANE Select | NP_000485.3:p.Gly1042= |