Linked Data
gnomAD v4:
8-38145221-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38145221C>T , CM000670.2:g.38145221C>T | GRCh38 |
| NC_000008.10:g.38002739C>T , CM000670.1:g.38002739C>T | GRCh37 |
| NC_000008.9:g.38121896C>T | NCBI36 |
| NG_011827.1:g.10862G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000276449.9:c.744+1G>A MANE Select | ENSP00000276449.3:n.744+1G>A | |
| ENST00000276449.8:c.744+1G>A | ENSP00000276449.3:n.744+1G>A | |
| ENST00000520114.1:n.1879G>A | ||
| ENST00000522050.1:c.586+742G>A | ||
| NM_000349.2:c.744+1G>A | NP_000340.2:n.744+1G>A | |
| XM_006716392.1:c.650+742G>A | XP_006716455.1:n.650+742G>A | |
| NM_000349.3:c.744+1G>A MANE Select | NP_000340.2:n.744+1G>A |