Linked Data
dbSNP Id:
rs1776802491
gnomAD v3:
6-31161835-G-A
gnomAD v4:
6-31161835-G-A
MyVariant Identifiers:
chr6:g.31129612G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31161835G>A , CM000668.2:g.31161835G>A | GRCh38 |
| NC_000006.11:g.31129612G>A , CM000668.1:g.31129612G>A | GRCh37 |
| NC_000006.10:g.31237591G>A | NCBI36 |
| NG_054878.1:g.1404C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000542218.2:c.627G>A | ENSP00000439397.2:p.Gly209= | |
| ENST00000706778.1:c.627G>A | ENSP00000516543.1:p.Gly209= | |
| ENST00000706779.1:c.627G>A | ENSP00000516544.1:p.Gly209= | |
| ENST00000706780.1:c.627G>A | ENSP00000516545.1:p.Gly209= | |
| ENST00000706781.1:c.627G>A | ENSP00000516546.1:p.Gly209= | |
| ENST00000706782.1:c.627G>A | ENSP00000516547.1:p.Gly209= | |
| ENST00000706783.1:c.458G>A | ENSP00000516548.1:p.Gly153Glu | |
| ENST00000706785.1:c.412G>A | ENSP00000516549.1:p.Gly138Arg | |
| ENST00000706786.1:c.458G>A | ENSP00000516550.1:p.Gly153Glu | |
| ENST00000706787.1:c.627G>A | ENSP00000516551.1:p.Gly209= | |
| ENST00000706788.1:n.578G>A | ||
| ENST00000376257.8:c.627G>A MANE Select | ENSP00000365433.3:p.Gly209= | |
| ENST00000376255.4:c.627G>A | ENSP00000365431.4:p.Gly209= | |
| ENST00000376257.7:c.627G>A | ENSP00000365433.3:p.Gly209= | |
| ENST00000496421.1:n.179G>A | ||
| ENST00000542218.1:c.387G>A | ENSP00000439397.1:p.Gly129= | |
| NM_001077511.1:c.627G>A | NP_001070979.1:p.Gly209= | |
| NM_007109.2:c.627G>A | NP_009040.2:p.Gly209= | |
| XM_005249334.2:c.627G>A | XP_005249391.1:p.Gly209= | |
| XM_011514829.1:c.627G>A | XP_011513131.1:p.Gly209= | |
| NM_001318908.1:c.627G>A | NP_001305837.1:p.Gly209= | |
| NM_007109.3:c.627G>A MANE Select | NP_009040.2:p.Gly209= | |
| NM_001077511.2:c.627G>A | NP_001070979.1:p.Gly209= | |
| NM_001318908.2:c.627G>A | NP_001305837.1:p.Gly209= |