Linked Data
gnomAD v4:
4-177442500-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.177442500C>T , CM000666.2:g.177442500C>T | GRCh38 |
| NC_000004.11:g.178363654C>T , CM000666.1:g.178363654C>T | GRCh37 |
| NC_000004.10:g.178600648C>T | NCBI36 |
| NG_011845.2:g.5004G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264595.6:c.-125G>A (AGA) | ENSP00000264595.2:n.-125G>A | |
| NM_000027.3:c.-125G>A (AGA) | NP_000018.2:n.-125G>A | |
| NM_001171988.1:c.-125G>A (AGA) | NP_001165459.1:n.-125G>A | |
| NR_033655.1:n.4G>A (AGA) | ||
| XM_006714123.2:c.-125G>A (AGA) | XP_006714186.1:n.-125G>A | |
| XR_001741929.1:n.1C>T (AGA-DT) |