Linked Data
gnomAD v4:
4-73404261-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73404261T>G , CM000666.2:g.73404261T>G | GRCh38 |
| NC_000004.11:g.74269978T>G , CM000666.1:g.74269978T>G | GRCh37 |
| NC_000004.10:g.74488842T>G | NCBI36 |
| NG_009291.1:g.5007T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000295897.8:c.-67T>G | ENSP00000295897.4:n.-67T>G | |
| ENST00000441319.5:c.48-108T>G | ENSP00000392541.1:n.48-108T>G | |
| ENST00000621628.4:c.-67T>G | ENSP00000480485.1:n.-67T>G | |
| NM_000477.5:c.-67T>G | NP_000468.1:n.-67T>G | |
| NM_000477.6:c.-67T>G | NP_000468.1:n.-67T>G |