Linked Data
gnomAD v4:
5-138946898-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.138946898C>T , CM000667.2:g.138946898C>T | GRCh38 |
| NC_000005.9:g.138282587C>T , CM000667.1:g.138282587C>T | GRCh37 |
| NC_000005.8:g.138310486C>T | NCBI36 |
| NG_008112.1:g.256479G>A | |
| NG_008112.2:g.256479G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394817.7:c.*219G>A MANE Select | ENSP00000378294.2:n.*219G>A | |
| ENST00000265195.9:c.*219G>A | ENSP00000265195.5:n.*219G>A | |
| ENST00000394817.6:c.*219G>A | ENSP00000378294.2:n.*219G>A | |
| NM_001037633.1:c.*219G>A | NP_001032722.1:n.*219G>A | |
| NM_022464.4:c.*219G>A | NP_071909.1:n.*219G>A | |
| XM_011543570.2:c.*219G>A | XP_011541872.1:n.*219G>A | |
| XM_024446164.1:c.*219G>A | XP_024301932.1:n.*219G>A | |
| NM_022464.5:c.*219G>A MANE Select | NP_071909.1:n.*219G>A | |
| NM_001037633.2:c.*219G>A | NP_001032722.1:n.*219G>A |