Linked Data
dbSNP Id:
rs1575712183
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240877455T>G , CM000664.2:g.240877455T>G | GRCh38 |
| NC_000002.11:g.241816872T>G , CM000664.1:g.241816872T>G | GRCh37 |
| NC_000002.10:g.241465545T>G | NCBI36 |
| NG_008005.1:g.13711T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.847-82T>G MANE Select | ENSP00000302620.3:n.847-82T>G | |
| ENST00000307503.3:c.847-82T>G | ENSP00000302620.3:n.847-82T>G | |
| ENST00000470255.1:n.543T>G | ||
| NM_000030.2:c.847-82T>G | NP_000021.1:n.847-82T>G | |
| NM_000030.3:c.847-82T>G MANE Select | NP_000021.1:n.847-82T>G |