MyVariant.info:
GRCh37
chr18:g.905125A>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.905124A>T , CM000680.2:g.905124A>T | GRCh38 |
| NC_000018.9:g.905125A>T , CM000680.1:g.905125A>T | GRCh37 |
| NC_000018.8:g.895125A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450565.8:c.-2+64A>T MANE Select | ENSP00000411658.3:n.-2+64A>T | |
| ENST00000450565.7:c.-2+64A>T | ENSP00000411658.3:n.-2+64A>T | |
| ENST00000579794.1:c.-263A>T | ENSP00000462647.1:n.-263A>T | |
| NM_001099733.1:c.-2+64A>T | NP_001093203.1:n.-2+64A>T | |
| XM_005258081.2:c.482+64A>T | XP_005258138.1:n.482+64A>T | |
| XM_005258081.4:c.416+64A>T | XP_005258138.2:n.416+64A>T | |
| NM_001099733.2:c.-2+64A>T MANE Select | NP_001093203.1:n.-2+64A>T |