Linked Data
ClinVar Variation Id:
2972715
ClinVar RCV Id:
RCV003837825
dbSNP Id:
rs919198041
gnomAD v3:
6-44313228-C-A
gnomAD v4:
6-44313228-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.44313228C>A , CM000668.2:g.44313228C>A | GRCh38 |
| NC_000006.11:g.44280965C>A , CM000668.1:g.44280965C>A | GRCh37 |
| NC_000006.10:g.44388943C>A | NCBI36 |
| NG_031952.1:g.5099G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000244571.5:c.96G>T (AARS2) MANE Select | ENSP00000244571.4:p.Ser32= | |
| ENST00000244571.4:c.96G>T (AARS2) | ENSP00000244571.4:p.Ser32= | |
| ENST00000505802.1:c.855+5586C>A | ||
| NM_020745.3:c.96G>T (AARS2) | NP_065796.1:p.Ser32= | |
| XM_005249245.2:c.96G>T (AARS2) | XP_005249302.1:p.Ser32= | |
| XM_011514764.1:c.96G>T (AARS2) | XP_011513066.1:p.Ser32= | |
| XR_241907.2:n.131G>T (AARS2) | ||
| XM_005249245.3:c.96G>T (AARS2) | XP_005249302.1:p.Ser32= | |
| XM_011514764.2:c.96G>T (AARS2) | XP_011513066.1:p.Ser32= | |
| NM_020745.4:c.96G>T (AARS2) MANE Select | NP_065796.2:p.Ser32= | |
| NM_001318876.2:c.946-128662C>A (POLR1C) | NP_001305805.1:n.946-128662C>A |