Linked Data
dbSNP Id:
rs544765632
gnomAD v2:
19-6713102-C-A
gnomAD v3:
19-6713091-C-A
gnomAD v4:
19-6713091-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713091C>A , CM000681.2:g.6713091C>A | GRCh38 |
| NC_000019.9:g.6713102C>A , CM000681.1:g.6713102C>A | GRCh37 |
| NC_000019.8:g.6664102C>A | NCBI36 |
| NG_009557.1:g.12561G>T , LRG_27:g.12561G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.880+98G>T | ENSP00000512083.1:n.880+98G>T | |
| ENST00000695654.1:c.127+98G>T | ENSP00000512085.1:n.127+98G>T | |
| ENST00000695692.1:n.327+98G>T | ||
| ENST00000245907.11:c.1003+98G>T MANE Select | ENSP00000245907.4:n.1003+98G>T | |
| ENST00000245907.10:c.1003+98G>T | ENSP00000245907.4:n.1003+98G>T | |
| ENST00000594270.5:n.127+98G>T | ||
| ENST00000595577.1:n.507+98G>T | ||
| ENST00000597442.5:n.253+98G>T | ||
| NM_000064.3:c.1003+98G>T | NP_000055.2:n.1003+98G>T | |
| NM_000064.4:c.1003+98G>T MANE Select | NP_000055.2:n.1003+98G>T |