Linked Data
dbSNP Id:
rs1403465089
gnomAD v2:
5-151230862-C-A
gnomAD v3:
5-151851301-C-A
gnomAD v4:
5-151851301-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.151851301C>A , CM000667.2:g.151851301C>A | GRCh38 |
| NC_000005.9:g.151230862C>A , CM000667.1:g.151230862C>A | GRCh37 |
| NC_000005.8:g.151211055C>A | NCBI36 |
| NG_011764.1:g.78536G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000274576.9:c.912+89G>T MANE Select | ENSP00000274576.5:n.912+89G>T | |
| ENST00000274576.8:c.912+89G>T | ENSP00000274576.4:n.912+89G>T | |
| ENST00000455880.2:c.912+89G>T | ENSP00000411593.2:n.912+89G>T | |
| ENST00000462581.6:c.*670+89G>T | ENSP00000430595.1:n.*670+89G>T | |
| ENST00000471351.2:n.1195+89G>T | ||
| NM_000171.3:c.912+89G>T | NP_000162.2:n.912+89G>T | |
| NM_001146040.1:c.912+89G>T | NP_001139512.1:n.912+89G>T | |
| NM_001292000.1:c.663+89G>T | NP_001278929.1:n.663+89G>T | |
| XM_005268412.2:c.912+89G>T | XP_005268469.1:n.912+89G>T | |
| NM_000171.4:c.912+89G>T MANE Select | NP_000162.2:n.912+89G>T | |
| NM_001146040.2:c.912+89G>T | NP_001139512.1:n.912+89G>T | |
| NM_001292000.2:c.663+89G>T | NP_001278929.1:n.663+89G>T |