Linked Data
dbSNP Id:
rs1703519524
gnomAD v3:
3-50345550-C-T
gnomAD v4:
3-50345550-C-T
MyVariant Identifiers:
chr3:g.50382981C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.50345550C>T , CM000665.2:g.50345550C>T | GRCh38 |
| NC_000003.11:g.50382981C>T , CM000665.1:g.50382981C>T | GRCh37 |
| NC_000003.10:g.50357985C>T | NCBI36 |
| NG_023270.1:g.387G>A | |
| NG_042828.1:g.5197G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000231749.8:c.30G>A MANE Select | ENSP00000231749.3:p.Gly10= | |
| ENST00000231749.7:c.30G>A | ENSP00000231749.3:p.Gly10= | |
| ENST00000360165.7:c.30G>A | ENSP00000353289.3:p.Gly10= | |
| ENST00000431869.1:c.30G>A | ENSP00000391545.1:p.Gly10= | |
| ENST00000442887.1:c.-53G>A | ENSP00000393687.1:n.-53G>A | |
| ENST00000443080.5:c.30G>A | ENSP00000415661.1:p.Gly10= | |
| ENST00000468182.1:n.132G>A | ||
| NM_001308379.1:c.30G>A | NP_001295308.1:p.Gly10= | |
| NM_015896.2:c.30G>A | NP_056980.2:p.Gly10= | |
| NM_015896.3:c.30G>A | NP_056980.2:p.Gly10= | |
| XM_005265216.2:c.-99G>A | XP_005265273.1:n.-99G>A | |
| XM_005265216.3:c.-99G>A | XP_005265273.1:n.-99G>A | |
| NM_015896.4:c.30G>A MANE Select | NP_056980.2:p.Gly10= | |
| NM_001308379.2:c.30G>A | NP_001295308.1:p.Gly10= |