Linked Data
MyVariant Identifiers:
chr1:g.55509680G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55044007G>T , CM000663.2:g.55044007G>T | GRCh38 |
| NC_000001.10:g.55509680G>T , CM000663.1:g.55509680G>T | GRCh37 |
| NC_000001.9:g.55282268G>T | NCBI36 |
| NG_009061.1:g.9461G>T , LRG_275:g.9461G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673913.2:c.372G>T | ENSP00000501161.2:p.Val124= | |
| ENST00000710286.1:c.729G>T | ENSP00000518176.1:p.Val243= | |
| ENST00000673662.1:n.42G>T | ||
| ENST00000673726.1:c.372G>T | ENSP00000501004.1:p.Val124= | |
| ENST00000673903.1:c.-4G>T | ENSP00000501257.1:n.-4G>T | |
| ENST00000302118.5:c.372G>T MANE Select | ENSP00000303208.5:p.Val124= | |
| NM_174936.3:c.372G>T , LRG_275t1:c.372G>T | NP_777596.2:p.Val124= | |
| NR_110451.1:n.182+3604G>T | ||
| NM_174936.4:c.372G>T MANE Select | NP_777596.2:p.Val124= | |
| NR_110451.2:n.182+3604G>T |