Linked Data
gnomAD v4:
4-67754371-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67754371T>G , CM000666.2:g.67754371T>G | GRCh38 |
| NC_000004.11:g.68620089T>G , CM000666.1:g.68620089T>G | GRCh37 |
| NC_000004.10:g.68302684T>G | NCBI36 |
| NG_009293.1:g.6716A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226413.5:c.-36A>C MANE Select | ENSP00000226413.5:n.-36A>C | |
| NM_000406.2:c.-36A>C | NP_000397.1:n.-36A>C | |
| NM_001012763.1:c.-36A>C | NP_001012781.1:n.-36A>C | |
| NM_000406.3:c.-36A>C MANE Select | NP_000397.1:n.-36A>C | |
| NM_001012763.2:c.-36A>C | NP_001012781.1:n.-36A>C |