Linked Data
dbSNP Id:
rs747911288
ExAC:
4:74270030 C / T
gnomAD v2:
4-74270030-C-T
gnomAD v4:
4-73404313-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73404313C>T , CM000666.2:g.73404313C>T | GRCh38 |
| NC_000004.11:g.74270030C>T , CM000666.1:g.74270030C>T | GRCh37 |
| NC_000004.10:g.74488894C>T | NCBI36 |
| NG_009291.1:g.5059C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000295897.9:c.-15C>T MANE Select | ENSP00000295897.4:n.-15C>T | |
| ENST00000295897.8:c.-15C>T | ENSP00000295897.4:n.-15C>T | |
| ENST00000401494.7:c.-15C>T | ENSP00000384695.3:n.-15C>T | |
| ENST00000415165.6:c.-15C>T | ENSP00000401820.2:n.-15C>T | |
| ENST00000441319.5:c.48-56C>T | ENSP00000392541.1:n.48-56C>T | |
| ENST00000476441.6:c.-15C>T | ENSP00000423727.1:n.-15C>T | |
| ENST00000503124.5:c.-195C>T | ENSP00000421027.1:n.-195C>T | |
| ENST00000509063.5:c.-15C>T | ENSP00000422784.1:n.-15C>T | |
| ENST00000510166.5:n.27C>T | ||
| ENST00000514786.1:n.25C>T | ||
| ENST00000515133.5:n.27C>T | ||
| ENST00000621085.4:c.-15C>T | ENSP00000483421.1:n.-15C>T | |
| ENST00000621628.4:c.-15C>T | ENSP00000480485.1:n.-15C>T | |
| NM_000477.5:c.-15C>T | NP_000468.1:n.-15C>T | |
| NM_000477.6:c.-15C>T | NP_000468.1:n.-15C>T | |
| NM_000477.7:c.-15C>T MANE Select | NP_000468.1:n.-15C>T |