Linked Data
dbSNP Id:
rs1046966691
gnomAD v4:
9-133352453-G-A
MyVariant Identifiers:
chr9:g.133352453G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133352453G>A , CM000671.2:g.133352453G>A | GRCh38 |
| NC_000009.10:g.135209129G>A | NCBI36 |
| NG_008477.1:g.9054C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371974.8:c.744C>T MANE Select | ENSP00000361042.3:p.Ala248= | |
| ENST00000371974.7:c.744C>T | ENSP00000361042.3:p.Ala248= | |
| ENST00000437995.1:n.654C>T | ||
| ENST00000495952.5:n.734C>T | ||
| ENST00000615505.4:c.417C>T | ENSP00000482067.1:p.Ala139= | |
| NM_001280787.1:c.417C>T | NP_001267716.1:p.Ala139= | |
| NM_003172.3:c.744C>T | NP_003163.1:p.Ala248= | |
| XM_011518942.1:c.417C>T | XP_011517244.1:p.Ala139= | |
| NM_003172.4:c.744C>T MANE Select | NP_003163.1:p.Ala248= |