Linked Data
gnomAD v4:
X-154379396-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154379396G>T , CM000685.2:g.154379396G>T | GRCh38 |
| NC_000023.10:g.153607756G>T , CM000685.1:g.153607756G>T | GRCh37 |
| NC_000023.9:g.153260950G>T | NCBI36 |
| NG_008677.1:g.9961G>T , LRG_745:g.9961G>T | |
| NG_011506.1:g.251C>A | |
| NG_011506.2:g.243C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369842.9:c.-89G>T MANE Select | ENSP00000358857.4:n.-89G>T | |
| ENST00000369835.3:c.-89G>T | ENSP00000358850.3:n.-89G>T | |
| ENST00000369842.8:c.-89G>T | ENSP00000358857.4:n.-89G>T | |
| ENST00000428228.5:c.-89G>T | ENSP00000401081.1:n.-89G>T | |
| ENST00000486738.5:n.56G>T | ||
| NM_000117.2:c.-89G>T , LRG_745t1:c.-89G>T | NP_000108.1:n.-89G>T | |
| XM_024452349.1:c.-297G>T | XP_024308117.1:n.-297G>T | |
| NM_000117.3:c.-89G>T MANE Select | NP_000108.1:n.-89G>T |