Linked Data
gnomAD v4:
1-115033356-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115033356A>G , CM000663.2:g.115033356A>G | GRCh38 |
| NC_000001.10:g.115575977A>G , CM000663.1:g.115575977A>G | GRCh37 |
| NC_000001.9:g.115377500A>G | NCBI36 |
| NG_015891.1:g.8563A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000256592.3:c.-1-6A>G MANE Select | ENSP00000256592.1:n.-1-6A>G | |
| ENST00000256592.2:c.-1-6A>G | ENSP00000256592.1:n.-1-6A>G | |
| NM_000549.4:c.-1-6A>G | NP_000540.2:n.-1-6A>G | |
| XM_011542065.1:c.-7A>G | XP_011540367.1:n.-7A>G | |
| XM_011542065.2:c.-7A>G | XP_011540367.1:n.-7A>G | |
| NM_000549.5:c.-1-6A>G MANE Select | NP_000540.2:n.-1-6A>G |