Linked Data
dbSNP Id:
rs1031100314
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57562972G>C , CM000682.2:g.57562972G>C | GRCh38 |
| NC_000020.10:g.56138028G>C , CM000682.1:g.56138028G>C | GRCh37 |
| NC_000020.9:g.55571434G>C | NCBI36 |
| NG_008205.1:g.6892G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.611-56G>C MANE Select | ENSP00000319814.4:n.611-56G>C | |
| ENST00000319441.5:c.611-56G>C | ENSP00000319814.4:n.611-56G>C | |
| ENST00000467047.1:n.1893G>C | ||
| ENST00000470051.1:n.139G>C | ||
| ENST00000498194.1:n.553-56G>C | ||
| NM_002591.3:c.611-56G>C | NP_002582.3:n.611-56G>C | |
| XM_011528839.1:c.215-56G>C | XP_011527141.1:n.215-56G>C | |
| XM_024451888.1:c.215-56G>C | XP_024307656.1:n.215-56G>C | |
| NM_002591.4:c.611-56G>C MANE Select | NP_002582.3:n.611-56G>C |