Linked Data
MyVariant Identifiers:
chr10:g.121431955C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119672443C>T , CM000672.2:g.119672443C>T | GRCh38 |
| NC_000010.10:g.121431955C>T , CM000672.1:g.121431955C>T | GRCh37 |
| NC_000010.9:g.121421945C>T | NCBI36 |
| NG_016125.1:g.26074C>T , LRG_742:g.26074C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.696C>T MANE Select | ENSP00000358081.4:p.His232= | |
| ENST00000369085.7:c.696C>T | ENSP00000358081.3:p.His232= | |
| ENST00000450186.1:c.522C>T | ENSP00000410036.1:p.His174= | |
| NM_004281.3:c.696C>T , LRG_742t1:c.696C>T | NP_004272.2:p.His232= | |
| XM_005270287.1:c.696C>T | XP_005270344.1:p.His232= | |
| XM_005270287.2:c.696C>T | XP_005270344.1:p.His232= | |
| NM_004281.4:c.696C>T MANE Select | NP_004272.2:p.His232= |