Linked Data
dbSNP Id:
rs1575707111
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240868890A>G , CM000664.2:g.240868890A>G | GRCh38 |
| NC_000002.11:g.241808307A>G , CM000664.1:g.241808307A>G | GRCh37 |
| NC_000002.10:g.241456980A>G | NCBI36 |
| NG_008005.1:g.5146A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.25A>G MANE Select | ENSP00000302620.3:p.Thr9Ala | |
| ENST00000307503.3:c.25A>G | ENSP00000302620.3:p.Thr9Ala | |
| ENST00000472436.1:n.45A>G | ||
| NM_000030.2:c.25A>G | NP_000021.1:p.Thr9Ala | |
| XR_924060.1:n.405+1343T>C | ||
| NM_000030.3:c.25A>G MANE Select | NP_000021.1:p.Thr9Ala |