Linked Data
dbSNP Id:
rs143665140
ExAC:
4:74279175 G / T
gnomAD v2:
4-74279175-G-T
gnomAD v4:
4-73413458-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73413458G>T , CM000666.2:g.73413458G>T | GRCh38 |
| NC_000004.11:g.74279175G>T , CM000666.1:g.74279175G>T | GRCh37 |
| NC_000004.10:g.74498039G>T | NCBI36 |
| NG_009291.1:g.14204G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000295897.9:c.882G>T MANE Select | ENSP00000295897.4:p.Ser294= | |
| ENST00000295897.8:c.882G>T | ENSP00000295897.4:p.Ser294= | |
| ENST00000401494.7:c.537G>T | ENSP00000384695.3:p.Ser179= | |
| ENST00000415165.6:c.306G>T | ENSP00000401820.2:p.Ser102= | |
| ENST00000476441.6:c.*161G>T | ENSP00000423727.1:n.*161G>T | |
| ENST00000484992.1:n.202G>T | ||
| ENST00000503124.5:c.432G>T | ENSP00000421027.1:p.Ser144= | |
| ENST00000505649.5:n.568G>T | ||
| ENST00000509063.5:c.882G>T | ENSP00000422784.1:p.Ser294= | |
| ENST00000511370.1:c.415G>T | ||
| ENST00000621085.4:c.491-1648G>T | ENSP00000483421.1:n.491-1648G>T | |
| ENST00000621628.4:c.487-1644G>T | ENSP00000480485.1:n.487-1644G>T | |
| NM_000477.5:c.882G>T | NP_000468.1:p.Ser294= | |
| NM_000477.6:c.882G>T | NP_000468.1:p.Ser294= | |
| NM_000477.7:c.882G>T MANE Select | NP_000468.1:p.Ser294= |