Linked Data
ClinVar Variation Id:
1100148
ClinVar RCV Id:
RCV001422664
dbSNP Id:
rs2134084242
MyVariant Identifiers:
chr10:g.104595081C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102835324C>T , CM000672.2:g.102835324C>T | GRCh38 |
| NC_000010.10:g.104595081C>T , CM000672.1:g.104595081C>T | GRCh37 |
| NC_000010.9:g.104585071C>T | NCBI36 |
| NG_007955.1:g.7210G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000369887.4:c.366G>A MANE Select | ENSP00000358903.3:p.Gln122= | |
| ENST00000638190.1:c.366G>A | ENSP00000492539.1:p.Gln122= | |
| ENST00000638272.1:c.297+1741G>A | ENSP00000491508.1:n.297+1741G>A | |
| ENST00000638971.1:c.366G>A | ENSP00000492313.1:p.Gln122= | |
| ENST00000639393.1:c.366G>A | ENSP00000492651.1:p.Gln122= | |
| ENST00000640633.1:n.128G>A | ||
| ENST00000369887.3:c.366G>A | ENSP00000358903.3:p.Gln122= | |
| ENST00000489268.1:n.620G>A | ||
| NM_000102.3:c.366G>A | NP_000093.1:p.Gln122= | |
| NM_000102.4:c.366G>A MANE Select | NP_000093.1:p.Gln122= |