Linked Data
ClinVar Variation Id:
2929622
ClinVar RCV Id:
RCV003784788
dbSNP Id:
rs1455139109
gnomAD v2:
10-121432123-C-T
gnomAD v3:
10-119672611-C-T
gnomAD v4:
10-119672611-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119672611C>T , CM000672.2:g.119672611C>T | GRCh38 |
| NC_000010.10:g.121432123C>T , CM000672.1:g.121432123C>T | GRCh37 |
| NC_000010.9:g.121422113C>T | NCBI36 |
| NG_016125.1:g.26242C>T , LRG_742:g.26242C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.864C>T MANE Select | ENSP00000358081.4:p.His288= | |
| ENST00000369085.7:c.864C>T | ENSP00000358081.3:p.His288= | |
| ENST00000450186.1:c.690C>T | ENSP00000410036.1:p.His230= | |
| NM_004281.3:c.864C>T , LRG_742t1:c.864C>T | NP_004272.2:p.His288= | |
| XM_005270287.1:c.864C>T | XP_005270344.1:p.His288= | |
| XM_005270287.2:c.864C>T | XP_005270344.1:p.His288= | |
| NM_004281.4:c.864C>T MANE Select | NP_004272.2:p.His288= |