Linked Data
dbSNP Id:
rs137853932
gnomAD v2:
19-18710374-C-T
gnomAD v4:
19-18599564-C-T
PubMed:
PMID:21370513
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18599564C>T , CM000681.2:g.18599564C>T | GRCh38 |
| NC_000019.9:g.18710374C>T , CM000681.1:g.18710374C>T | GRCh37 |
| NC_000019.8:g.18571374C>T | NCBI36 |
| NG_013370.1:g.12287G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000684169.1:c.397+1G>A | ENSP00000506849.1:n.397+1G>A | |
| ENST00000392386.8:c.397+1G>A MANE Select | ENSP00000376188.2:n.397+1G>A | |
| ENST00000392386.7:c.397+1G>A | ENSP00000376188.2:n.397+1G>A | |
| NM_004750.4:c.397+1G>A | NP_004741.1:n.397+1G>A | |
| XM_011528422.1:c.331+1G>A | XP_011526724.1:n.331+1G>A | |
| XM_011528423.1:c.397+1G>A | XP_011526725.1:n.397+1G>A | |
| XM_011528424.1:c.331+1G>A | XP_011526726.1:n.331+1G>A | |
| XM_011528422.2:c.331+1G>A | XP_011526724.1:n.331+1G>A | |
| XM_011528423.2:c.397+1G>A | XP_011526725.1:n.397+1G>A | |
| XM_011528424.3:c.331+1G>A | XP_011526726.1:n.331+1G>A | |
| NM_004750.5:c.397+1G>A MANE Select | NP_004741.1:n.397+1G>A |