Linked Data
dbSNP Id:
rs1424655550
gnomAD v2:
4-74270315-A-T
gnomAD v3:
4-73404598-A-T
gnomAD v4:
4-73404598-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73404598A>T , CM000666.2:g.73404598A>T | GRCh38 |
| NC_000004.11:g.74270315A>T , CM000666.1:g.74270315A>T | GRCh37 |
| NC_000004.10:g.74489179A>T | NCBI36 |
| NG_009291.1:g.5344A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295897.9:c.79+192A>T MANE Select | ENSP00000295897.4:n.79+192A>T | |
| ENST00000295897.8:c.79+192A>T | ENSP00000295897.4:n.79+192A>T | |
| ENST00000401494.7:c.79+192A>T | ENSP00000384695.3:n.79+192A>T | |
| ENST00000415165.6:c.79+192A>T | ENSP00000401820.2:n.79+192A>T | |
| ENST00000441319.5:c.85+192A>T | ENSP00000392541.1:n.85+192A>T | |
| ENST00000476441.6:c.79+192A>T | ENSP00000423727.1:n.79+192A>T | |
| ENST00000503124.5:c.-102+192A>T | ENSP00000421027.1:n.-102+192A>T | |
| ENST00000509063.5:c.79+192A>T | ENSP00000422784.1:n.79+192A>T | |
| ENST00000510166.5:n.120+192A>T | ||
| ENST00000514786.1:n.48+262A>T | ||
| ENST00000515133.5:n.120+192A>T | ||
| ENST00000621085.4:c.79+192A>T | ENSP00000483421.1:n.79+192A>T | |
| ENST00000621628.4:c.79+192A>T | ENSP00000480485.1:n.79+192A>T | |
| NM_000477.5:c.79+192A>T | NP_000468.1:n.79+192A>T | |
| NM_000477.6:c.79+192A>T | NP_000468.1:n.79+192A>T | |
| NM_000477.7:c.79+192A>T MANE Select | NP_000468.1:n.79+192A>T |