Linked Data
gnomAD v4:
X-54465908-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.54465908T>C , CM000685.2:g.54465908T>C | GRCh38 |
| NC_000023.10:g.54492341T>C , CM000685.1:g.54492341T>C | GRCh37 |
| NC_000023.9:g.54509066T>C | NCBI36 |
| NG_008054.1:g.35259A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375135.4:c.1341-56A>G MANE Select | ENSP00000364277.3:n.1341-56A>G | |
| ENST00000375135.3:c.1341-56A>G | ENSP00000364277.3:n.1341-56A>G | |
| NM_004463.2:c.1341-56A>G | NP_004454.2:n.1341-56A>G | |
| NM_004463.3:c.1341-56A>G MANE Select | NP_004454.2:n.1341-56A>G |