Linked Data
gnomAD v4:
18-31498199-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31498199G>T , CM000680.2:g.31498199G>T | GRCh38 |
| NC_000018.9:g.29078162G>T , CM000680.1:g.29078162G>T | GRCh37 |
| NC_000018.8:g.27332160G>T | NCBI36 |
| NG_007072.3:g.4958G>T , LRG_397:g.4958G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261590.13:c.-53G>T MANE Select | ENSP00000261590.8:n.-53G>T | |
| ENST00000261590.12:c.-53G>T | ENSP00000261590.8:n.-53G>T | |
| NM_001943.3:c.-53G>T , LRG_397t1:c.-53G>T | NP_001934.2:n.-53G>T | |
| NM_001943.4:c.-53G>T | NP_001934.2:n.-53G>T | |
| NM_001943.5:c.-53G>T MANE Select | NP_001934.2:n.-53G>T |