Linked Data
dbSNP Id:
rs776810332
ExAC:
5:138282914 C / G
gnomAD v2:
5-138282914-C-G
gnomAD v4:
5-138947225-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.138947225C>G , CM000667.2:g.138947225C>G | GRCh38 |
| NC_000005.9:g.138282914C>G , CM000667.1:g.138282914C>G | GRCh37 |
| NC_000005.8:g.138310813C>G | NCBI36 |
| NG_008112.1:g.256152G>C | |
| NG_008112.2:g.256152G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394817.7:c.1278G>C MANE Select | ENSP00000378294.2:p.Gln426His | |
| ENST00000265195.9:c.1278G>C | ENSP00000265195.5:p.Gln426His | |
| ENST00000394817.6:c.1278G>C | ENSP00000378294.2:p.Gln426His | |
| ENST00000509534.5:c.1299G>C | ENSP00000426858.1:p.Gln433His | |
| ENST00000515008.1:n.613G>C | ||
| NM_001037633.1:c.1278G>C | NP_001032722.1:p.Gln426His | |
| NM_022464.4:c.1278G>C | NP_071909.1:p.Gln426His | |
| XM_011543570.1:c.1308G>C | XP_011541872.1:p.Gln436His | |
| XM_011543570.2:c.1308G>C | XP_011541872.1:p.Gln436His | |
| XM_024446164.1:c.1278G>C | XP_024301932.1:p.Gln426His | |
| NM_022464.5:c.1278G>C MANE Select | NP_071909.1:p.Gln426His | |
| NM_001037633.2:c.1278G>C | NP_001032722.1:p.Gln426His |