Linked Data
ClinVar Variation Id:
458757
dbSNP Id:
rs1348701377
gnomAD v2:
5-127674745-C-T
gnomAD v4:
5-128339053-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128339053C>T , CM000667.2:g.128339053C>T | GRCh38 |
| NC_000005.9:g.127674745C>T , CM000667.1:g.127674745C>T | GRCh37 |
| NC_000005.8:g.127702644C>T | NCBI36 |
| NG_008750.1:g.203991G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703783.1:n.136G>A | ||
| ENST00000703785.1:n.217G>A | ||
| ENST00000262464.9:c.3352G>A MANE Select | ENSP00000262464.4:p.Glu1118Lys | |
| ENST00000262464.8:c.3352G>A | ENSP00000262464.4:p.Glu1118Lys | |
| ENST00000507835.5:c.-99G>A | ENSP00000426839.1:n.-99G>A | |
| ENST00000508053.5:c.3352G>A | ENSP00000424571.1:p.Glu1118Lys | |
| ENST00000508989.5:c.3253G>A | ENSP00000425596.1:p.Glu1085Lys | |
| ENST00000619499.4:c.3349G>A | ENSP00000482132.1:p.Glu1117Lys | |
| NM_001999.3:c.3352G>A | NP_001990.2:p.Glu1118Lys | |
| XM_017009228.2:c.3199G>A | XP_016864717.1:p.Glu1067Lys | |
| NM_001999.4:c.3352G>A MANE Select | NP_001990.2:p.Glu1118Lys |