Linked Data
dbSNP Id:
rs1003141068
gnomAD v2:
19-6697892-G-A
gnomAD v3:
19-6697881-G-A
gnomAD v4:
19-6697881-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6697881G>A , CM000681.2:g.6697881G>A | GRCh38 |
| NC_000019.9:g.6697892G>A , CM000681.1:g.6697892G>A | GRCh37 |
| NC_000019.8:g.6648892G>A | NCBI36 |
| NG_009557.1:g.27771C>T , LRG_27:g.27771C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695651.1:n.789-87C>T | ||
| ENST00000695652.1:c.2318-87C>T | ENSP00000512083.1:n.2318-87C>T | |
| ENST00000695653.1:c.350-87C>T | ENSP00000512084.1:n.350-87C>T | |
| ENST00000695654.1:c.1565-87C>T | ENSP00000512085.1:n.1565-87C>T | |
| ENST00000695655.1:c.1382-87C>T | ENSP00000512086.1:n.1382-87C>T | |
| ENST00000695692.1:n.1805-87C>T | ||
| ENST00000245907.11:c.2441-87C>T MANE Select | ENSP00000245907.4:n.2441-87C>T | |
| ENST00000245907.10:c.2441-87C>T | ENSP00000245907.4:n.2441-87C>T | |
| ENST00000602053.1:n.489-87C>T | ||
| NM_000064.3:c.2441-87C>T | NP_000055.2:n.2441-87C>T | |
| NM_000064.4:c.2441-87C>T MANE Select | NP_000055.2:n.2441-87C>T |