Linked Data
ClinVar Variation Id:
576158
ClinVar RCV Id:
RCV000698584
dbSNP Id:
rs1172460177
gnomAD v2:
5-13769143-T-C
gnomAD v3:
5-13769034-T-C
gnomAD v4:
5-13769034-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13769034T>C , CM000667.2:g.13769034T>C | GRCh38 |
| NC_000005.9:g.13769143T>C , CM000667.1:g.13769143T>C | GRCh37 |
| NC_000005.8:g.13822143T>C | NCBI36 |
| NG_013081.1:g.180447A>G | |
| NG_013081.2:g.180447A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.9823A>G MANE Select | ENSP00000265104.4:p.Lys3275Glu | |
| ENST00000681290.1:c.9778A>G | ENSP00000505288.1:p.Lys3260Glu | |
| ENST00000265104.4:c.9823A>G | ENSP00000265104.4:p.Lys3275Glu | |
| ENST00000504001.3:n.535A>G | ||
| NM_001369.2:c.9823A>G | NP_001360.1:p.Lys3275Glu | |
| XM_005248262.2:c.9778A>G | XP_005248319.1:p.Lys3260Glu | |
| XM_005248262.3:c.9931A>G | XP_005248319.2:p.Lys3311Glu | |
| XM_017009177.1:c.9931A>G | XP_016864666.1:p.Lys3311Glu | |
| XM_017009178.1:c.8836A>G | XP_016864667.1:p.Lys2946Glu | |
| XM_017009179.2:c.8836A>G | XP_016864668.1:p.Lys2946Glu | |
| XM_017009180.1:c.9931A>G | XP_016864669.1:p.Lys3311Glu | |
| XM_017009181.1:c.9931A>G | XP_016864670.1:p.Lys3311Glu | |
| XM_017009182.1:c.9931A>G | XP_016864671.1:p.Lys3311Glu | |
| XM_017009185.1:c.5020A>G | XP_016864674.1:p.Lys1674Glu | |
| XM_017009186.1:c.4573A>G | XP_016864675.1:p.Lys1525Glu | |
| XM_017009188.1:c.3910A>G | XP_016864677.1:p.Lys1304Glu | |
| XM_024454388.1:c.8836A>G | XP_024310156.1:p.Lys2946Glu | |
| XM_024454389.1:c.8425A>G | XP_024310157.1:p.Lys2809Glu | |
| NM_001369.3:c.9823A>G MANE Select | NP_001360.1:p.Lys3275Glu |