Linked Data
dbSNP Id:
rs1358890634
gnomAD v3:
6-44311038-G-T
gnomAD v4:
6-44311038-G-T
MyVariant Identifiers:
chr6:g.44278775G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.44311038G>T , CM000668.2:g.44311038G>T | GRCh38 |
| NC_000006.11:g.44278775G>T , CM000668.1:g.44278775G>T | GRCh37 |
| NC_000006.10:g.44386753G>T | NCBI36 |
| NG_031952.1:g.7289C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000244571.5:c.705C>A (AARS2) MANE Select | ENSP00000244571.4:p.Pro235= | |
| ENST00000244571.4:c.705C>A (AARS2) | ENSP00000244571.4:p.Pro235= | |
| ENST00000505802.1:c.855+3396G>T | ||
| NM_020745.3:c.705C>A (AARS2) | NP_065796.1:p.Pro235= | |
| XM_005249245.2:c.705C>A (AARS2) | XP_005249302.1:p.Pro235= | |
| XM_011514764.1:c.705C>A (AARS2) | XP_011513066.1:p.Pro235= | |
| XR_241907.2:n.740C>A (AARS2) | ||
| XM_005249245.3:c.705C>A (AARS2) | XP_005249302.1:p.Pro235= | |
| XM_011514764.2:c.705C>A (AARS2) | XP_011513066.1:p.Pro235= | |
| XM_017011112.1:c.-314C>A (AARS2) | XP_016866601.1:n.-314C>A | |
| NM_020745.4:c.705C>A (AARS2) MANE Select | NP_065796.2:p.Pro235= | |
| NM_001318876.2:c.946-130852G>T (POLR1C) | NP_001305805.1:n.946-130852G>T |