Linked Data
MyVariant Identifiers:
chr1:g.152276757C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152304281C>T , CM000663.2:g.152304281C>T | GRCh38 |
| NC_000001.10:g.152276757C>T , CM000663.1:g.152276757C>T | GRCh37 |
| NC_000001.9:g.150543381C>T | NCBI36 |
| NG_016190.1:g.25923G>A , LRG_1028:g.25923G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368799.2:c.10605G>A MANE Select | ENSP00000357789.1:p.Gln3535= | |
| ENST00000368799.1:c.10605G>A | ENSP00000357789.1:p.Gln3535= | |
| NM_002016.1:c.10605G>A , LRG_1028t1:c.10605G>A | NP_002007.1:p.Gln3535= | |
| XM_011509329.1:c.9109-448G>A | XP_011507631.1:n.9109-448G>A | |
| NM_002016.2:c.10605G>A MANE Select | NP_002007.1:p.Gln3535= |