Linked Data
MyVariant Identifiers:
chr8:g.37823700G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37966182G>A , CM000670.2:g.37966182G>A | GRCh38 |
| NC_000008.10:g.37823700G>A , CM000670.1:g.37823700G>A | GRCh37 |
| NC_000008.9:g.37942857G>A | NCBI36 |
| NG_011936.1:g.5485C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000345060.5:c.288C>T MANE Select | ENSP00000343782.3:p.Thr96= | |
| ENST00000520341.2:n.416C>T | ||
| ENST00000345060.4:c.288C>T | ENSP00000343782.3:p.Thr96= | |
| ENST00000614635.1:c.288C>T | ENSP00000480325.1:p.Thr96= | |
| NM_000025.2:c.288C>T | NP_000016.1:p.Thr96= | |
| NM_000025.3:c.288C>T MANE Select | NP_000016.1:p.Thr96= |