Linked Data
ClinVar Variation Id:
319224
dbSNP Id:
rs150810544
ExAC:
16:4387381 C / T
gnomAD v2:
16-4387381-C-T
gnomAD v3:
16-4337380-C-T
gnomAD v4:
16-4337380-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.4337380C>T , CM000678.2:g.4337380C>T | GRCh38 |
| NC_000016.9:g.4387381C>T , CM000678.1:g.4387381C>T | GRCh37 |
| NC_000016.8:g.4327382C>T | NCBI36 |
| NG_016391.1:g.10157C>T | |
| NG_016391.2:g.27620C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000433375.2:c.1431C>T (GLIS2) MANE Select | ENSP00000395547.1:p.Pro477= | |
| ENST00000262366.7:c.1431C>T (GLIS2) | ENSP00000262366.3:p.Pro477= | |
| ENST00000433375.1:c.1431C>T (GLIS2) | ENSP00000395547.1:p.Pro477= | |
| ENST00000577031.5:c.291+3540G>A (PAM16) | ENSP00000459113.1:n.291+3540G>A | |
| NM_032575.2:c.1431C>T (GLIS2) | NP_115964.2:p.Pro477= | |
| XM_005255641.3:c.1431C>T (GLIS2) | XP_005255698.1:p.Pro477= | |
| XM_005255642.2:c.1431C>T (GLIS2) | XP_005255699.1:p.Pro477= | |
| NM_001318918.1:c.1431C>T (GLIS2) | NP_001305847.1:p.Pro477= | |
| XM_005255641.4:c.1431C>T (GLIS2) | XP_005255698.1:p.Pro477= | |
| NM_032575.3:c.1431C>T (GLIS2) MANE Select | NP_115964.2:p.Pro477= | |
| NM_001318918.2:c.1431C>T (GLIS2) | NP_001305847.1:p.Pro477= |