Linked Data
dbSNP Id:
rs747374489
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869239T>A , CM000664.2:g.240869239T>A | GRCh38 |
| NC_000002.11:g.241808656T>A , CM000664.1:g.241808656T>A | GRCh37 |
| NC_000002.10:g.241457329T>A | NCBI36 |
| NG_008005.1:g.5495T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.235T>A MANE Select | ENSP00000302620.3:p.Ser79Thr | |
| ENST00000307503.3:c.235T>A | ENSP00000302620.3:p.Ser79Thr | |
| ENST00000472436.1:n.255T>A | ||
| NM_000030.2:c.235T>A | NP_000021.1:p.Ser79Thr | |
| XR_924060.1:n.405+994A>T | ||
| NM_000030.3:c.235T>A MANE Select | NP_000021.1:p.Ser79Thr |