Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.81207309A>T , CM000667.2:g.81207309A>T | GRCh38 |
| NC_000005.9:g.80503128A>T , CM000667.1:g.80503128A>T | GRCh37 |
| NC_000005.8:g.80538884A>T | NCBI36 |
| NG_030334.1:g.251621A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265080.9:c.3031A>T MANE Select | ENSP00000265080.4:p.Thr1011Ser | |
| ENST00000265080.8:c.3031A>T | ENSP00000265080.4:p.Thr1011Ser | |
| ENST00000503795.1:c.3031A>T | ENSP00000421771.1:p.Thr1011Ser | |
| NM_006909.2:c.3031A>T | NP_008840.1:p.Thr1011Ser | |
| XM_017009682.2:c.2746A>T | XP_016865171.1:p.Thr916Ser | |
| XR_002956166.1:n.3147A>T | ||
| NM_006909.3:c.3031A>T MANE Select | NP_008840.1:p.Thr1011Ser |