Linked Data
dbSNP Id:
rs1049678448
gnomAD v2:
11-110331531-G-T
gnomAD v3:
11-110460807-G-T
gnomAD v4:
11-110460807-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.110460807G>T , CM000673.2:g.110460807G>T | GRCh38 |
| NC_000011.9:g.110331531G>T , CM000673.1:g.110331531G>T | GRCh37 |
| NC_000011.8:g.109836741G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260270.3:c.441-1547G>T MANE Select | ENSP00000260270.2:n.441-1547G>T | |
| ENST00000260270.2:c.441-1547G>T | ENSP00000260270.2:n.441-1547G>T | |
| NM_004109.4:c.441-1547G>T | NP_004100.1:n.441-1547G>T | |
| NM_004109.5:c.441-1547G>T MANE Select | NP_004100.1:n.441-1547G>T |