Linked Data
gnomAD v4:
2-240873148-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240873148C>A , CM000664.2:g.240873148C>A | GRCh38 |
| NC_000002.11:g.241812565C>A , CM000664.1:g.241812565C>A | GRCh37 |
| NC_000002.10:g.241461238C>A | NCBI36 |
| NG_008005.1:g.9404C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.595+99C>A MANE Select | ENSP00000302620.3:n.595+99C>A | |
| ENST00000307503.3:c.595+99C>A | ENSP00000302620.3:n.595+99C>A | |
| ENST00000472436.1:n.714C>A | ||
| ENST00000476698.1:n.332+99C>A | ||
| NM_000030.2:c.595+99C>A | NP_000021.1:n.595+99C>A | |
| NM_000030.3:c.595+99C>A MANE Select | NP_000021.1:n.595+99C>A |