Linked Data
dbSNP Id:
rs1212689998
gnomAD v2:
6-31238477-C-A
gnomAD v3:
6-31270700-C-A
gnomAD v4:
6-31270700-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31270700C>A , CM000668.2:g.31270700C>A | GRCh38 |
| NC_000006.11:g.31238477C>A , CM000668.1:g.31238477C>A | GRCh37 |
| NC_000006.10:g.31346456C>A | NCBI36 |
| NG_029422.2:g.6432G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.620-215G>T MANE Select | ENSP00000365402.5:n.620-215G>T | |
| ENST00000376228.9:c.620-215G>T | ENSP00000365402.5:n.620-215G>T | |
| ENST00000376237.8:c.*207-215G>T | ENSP00000365412.4:n.*207-215G>T | |
| ENST00000383329.7:c.620-215G>T | ENSP00000372819.3:n.620-215G>T | |
| ENST00000415537.1:c.618-215G>T | ||
| ENST00000487245.5:n.979-215G>T | ||
| ENST00000495835.1:n.809-215G>T | ||
| NM_002117.5:c.620-215G>T | NP_002108.4:n.620-215G>T | |
| NM_002117.6:c.620-215G>T MANE Select | NP_002108.4:n.620-215G>T |