Linked Data
dbSNP Id:
rs765149589
ExAC:
6:44280958 G / C
gnomAD v2:
6-44280958-G-C
gnomAD v4:
6-44313221-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.44313221G>C , CM000668.2:g.44313221G>C | GRCh38 |
| NC_000006.11:g.44280958G>C , CM000668.1:g.44280958G>C | GRCh37 |
| NC_000006.10:g.44388936G>C | NCBI36 |
| NG_031952.1:g.5106C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000244571.5:c.103C>G (AARS2) MANE Select | ENSP00000244571.4:p.Pro35Ala | |
| ENST00000244571.4:c.103C>G (AARS2) | ENSP00000244571.4:p.Pro35Ala | |
| ENST00000505802.1:c.855+5579G>C | ||
| NM_020745.3:c.103C>G (AARS2) | NP_065796.1:p.Pro35Ala | |
| XM_005249245.2:c.103C>G (AARS2) | XP_005249302.1:p.Pro35Ala | |
| XM_011514764.1:c.103C>G (AARS2) | XP_011513066.1:p.Pro35Ala | |
| XR_241907.2:n.138C>G (AARS2) | ||
| XM_005249245.3:c.103C>G (AARS2) | XP_005249302.1:p.Pro35Ala | |
| XM_011514764.2:c.103C>G (AARS2) | XP_011513066.1:p.Pro35Ala | |
| NM_020745.4:c.103C>G (AARS2) MANE Select | NP_065796.2:p.Pro35Ala | |
| NM_001318876.2:c.946-128669G>C (POLR1C) | NP_001305805.1:n.946-128669G>C |