Linked Data
dbSNP Id:
rs1555211323
gnomAD v3:
10-47350263-G-C
gnomAD v4:
10-47350263-G-C
MyVariant Identifiers:
chr10:g.48389099C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.47350263G>C , CM000672.2:g.47350263G>C | GRCh38 |
| NC_000010.10:g.48389099C>G , CM000672.1:g.48389099C>G | GRCh37 |
| NC_000010.9:g.48009105C>G | NCBI36 |
| NG_029718.1:g.6893G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000584701.2:c.1779G>C MANE Select | ENSP00000463151.1:p.Val593= | |
| ENST00000584701.1:c.1779G>C | ENSP00000463151.1:p.Val593= | |
| NM_002900.2:c.1779G>C | NP_002891.1:p.Val593= | |
| NM_002900.3:c.1779G>C MANE Select | NP_002891.1:p.Val593= |