Linked Data
dbSNP Id:
rs1689367108
gnomAD v3:
2-176093649-C-T
gnomAD v4:
2-176093649-C-T
MyVariant Identifiers:
chr2:g.176958377C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.176093649C>T , CM000664.2:g.176093649C>T | GRCh38 |
| NC_000002.11:g.176958377C>T , CM000664.1:g.176958377C>T | GRCh37 |
| NC_000002.10:g.176666623C>T | NCBI36 |
| NG_008137.1:g.5846C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392539.4:c.759C>T MANE Select | ENSP00000376322.3:p.His253= | |
| ENST00000392539.3:c.759C>T | ENSP00000376322.3:p.His253= | |
| NM_000523.3:c.759C>T | NP_000514.2:p.His253= | |
| XM_011511068.1:c.725-831C>T | XP_011509370.1:n.725-831C>T | |
| XM_011511068.2:c.725-831C>T | XP_011509370.1:n.725-831C>T | |
| NM_000523.4:c.759C>T MANE Select | NP_000514.2:p.His253= |