Linked Data
dbSNP Id:
rs1329637860
gnomAD v2:
2-108994889-T-C
gnomAD v3:
2-108378433-T-C
gnomAD v4:
2-108378433-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.108378433T>C , CM000664.2:g.108378433T>C | GRCh38 |
| NC_000002.11:g.108994889T>C , CM000664.1:g.108994889T>C | GRCh37 |
| NC_000002.10:g.108361321T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272452.7:c.96T>C MANE Select | ENSP00000272452.2:p.Cys32= | |
| ENST00000272452.6:c.96T>C | ENSP00000272452.2:p.Cys32= | |
| ENST00000409309.3:c.96T>C | ENSP00000387225.3:p.Cys32= | |
| ENST00000494122.1:n.523T>C | ||
| NM_006588.2:c.96T>C | NP_006579.2:p.Cys32= | |
| XM_005263919.2:c.96T>C | XP_005263976.1:p.Cys32= | |
| NM_001321770.1:c.96T>C | NP_001308699.1:p.Cys32= | |
| NM_006588.3:c.96T>C | NP_006579.2:p.Cys32= | |
| NR_135776.1:n.523T>C | ||
| NR_135779.1:n.523T>C | ||
| XM_017003807.1:c.-225T>C | XP_016859296.1:n.-225T>C | |
| NM_006588.4:c.96T>C MANE Select | NP_006579.2:p.Cys32= | |
| NM_001321770.2:c.96T>C | NP_001308699.1:p.Cys32= | |
| NR_135776.2:n.480T>C | ||
| NR_135779.2:n.480T>C |