Linked Data
dbSNP Id:
rs1832526420
gnomAD v3:
10-3781756-T-A
gnomAD v4:
10-3781756-T-A
MyVariant Identifiers:
chr10:g.3823948T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.3781756T>A , CM000672.2:g.3781756T>A | GRCh38 |
| NC_000010.10:g.3823948T>A , CM000672.1:g.3823948T>A | GRCh37 |
| NC_000010.9:g.3813948T>A | NCBI36 |
| NG_012277.1:g.8526A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000497571.6:c.561A>T MANE Select | ENSP00000419923.1:p.Gly187= | |
| ENST00000173785.4:n.257+39A>T | ||
| ENST00000469435.1:c.561A>T | ENSP00000419079.1:p.Gly187= | |
| ENST00000497571.5:c.561A>T | ENSP00000419923.1:p.Gly187= | |
| ENST00000542957.1:c.561A>T | ENSP00000445301.1:p.Gly187= | |
| NM_001160124.1:c.550+11A>T | NP_001153596.1:n.550+11A>T | |
| NM_001160125.1:c.561A>T | NP_001153597.1:p.Gly187= | |
| NM_001300.5:c.561A>T | NP_001291.3:p.Gly187= | |
| NR_027653.1:n.789+39A>T | ||
| NM_001300.6:c.561A>T MANE Select | NP_001291.3:p.Gly187= | |
| NM_001160124.2:c.550+11A>T | NP_001153596.1:n.550+11A>T | |
| NR_027653.2:n.717+39A>T | ||
| NM_001160125.2:c.561A>T | NP_001153597.1:p.Gly187= |