Linked Data
gnomAD v4:
20-10656267-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10656267T>G , CM000682.2:g.10656267T>G | GRCh38 |
| NC_000020.10:g.10636915T>G , CM000682.1:g.10636915T>G | GRCh37 |
| NC_000020.9:g.10584915T>G | NCBI36 |
| NG_007496.1:g.22780A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.755+131A>C MANE Select | ENSP00000254958.4:n.755+131A>C | |
| ENST00000254958.9:c.755+131A>C | ENSP00000254958.4:n.755+131A>C | |
| ENST00000423891.6:n.621+131A>C | ||
| NM_000214.2:c.755+131A>C | NP_000205.1:n.755+131A>C | |
| NM_000214.3:c.755+131A>C MANE Select | NP_000205.1:n.755+131A>C |