Linked Data
MyVariant Identifiers:
chr1:g.55509701G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55044028G>C , CM000663.2:g.55044028G>C | GRCh38 |
| NC_000001.10:g.55509701G>C , CM000663.1:g.55509701G>C | GRCh37 |
| NC_000001.9:g.55282289G>C | NCBI36 |
| NG_009061.1:g.9482G>C , LRG_275:g.9482G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673913.2:c.393G>C | ENSP00000501161.2:p.Leu131= | |
| ENST00000710286.1:c.750G>C | ENSP00000518176.1:p.Leu250= | |
| ENST00000673662.1:n.63G>C | ||
| ENST00000673726.1:c.393G>C | ENSP00000501004.1:p.Leu131= | |
| ENST00000673903.1:c.18G>C | ENSP00000501257.1:p.Leu6= | |
| ENST00000302118.5:c.393G>C MANE Select | ENSP00000303208.5:p.Leu131= | |
| NM_174936.3:c.393G>C , LRG_275t1:c.393G>C | NP_777596.2:p.Leu131= | |
| NR_110451.1:n.182+3625G>C | ||
| NM_174936.4:c.393G>C MANE Select | NP_777596.2:p.Leu131= | |
| NR_110451.2:n.182+3625G>C |