Linked Data
ClinVar Variation Id:
657239
ClinVar RCV Id:
RCV003655289
dbSNP Id:
rs1593069244
gnomAD v4:
12-132672226-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.132672226T>C , CM000674.2:g.132672226T>C | GRCh38 |
| NC_000012.11:g.133248812T>C , CM000674.1:g.133248812T>C | GRCh37 |
| NC_000012.10:g.131758885T>C | NCBI36 |
| NG_033840.1:g.20299A>G , LRG_789:g.20299A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000539215.6:c.538A>G | ||
| ENST00000699982.1:c.1637A>G | ||
| ENST00000699983.1:c.1637A>G | ||
| ENST00000699984.1:c.1637A>G | ||
| ENST00000320574.10:c.1783A>G MANE Select | ENSP00000322570.5:p.Asn595Asp | |
| ENST00000672742.1:c.*1285A>G | ENSP00000500279.1:n.*1285A>G | |
| ENST00000320574.9:c.1783A>G | ENSP00000322570.5:p.Asn595Asp | |
| ENST00000535270.5:c.1702A>G | ENSP00000445753.1:p.Asn568Asp | |
| ENST00000537064.5:c.*830A>G | ENSP00000442578.1:n.*830A>G | |
| NM_006231.3:c.1783A>G , LRG_789t1:c.1783A>G | NP_006222.2:p.Asn595Asp | |
| XM_011534795.1:c.1783A>G | XP_011533097.1:p.Asn595Asp | |
| XM_011534796.1:c.1654A>G | XP_011533098.1:p.Asn552Asp | |
| XM_011534797.1:c.862A>G | XP_011533099.1:p.Asn288Asp | |
| XM_011534798.1:c.445A>G | XP_011533100.1:p.Asn149Asp | |
| XM_011534799.1:c.1783A>G | XP_011533101.1:p.Asn595Asp | |
| XM_011534800.1:c.1783A>G | XP_011533102.1:p.Asn595Asp | |
| XM_011534801.1:c.1783A>G | XP_011533103.1:p.Asn595Asp | |
| XR_941395.1:n.1992A>G | ||
| XM_011534795.3:c.1783A>G | XP_011533097.1:p.Asn595Asp | |
| XM_011534797.3:c.862A>G | XP_011533099.1:p.Asn288Asp | |
| XM_011534799.2:c.1783A>G | XP_011533101.1:p.Asn595Asp | |
| XR_002957338.1:n.1987A>G | ||
| XR_002957339.1:n.1987A>G | ||
| XR_941395.2:n.1987A>G | ||
| NM_006231.4:c.1783A>G MANE Select | NP_006222.2:p.Asn595Asp |