Linked Data
dbSNP Id:
rs16892496
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.109097622A>T , CM000670.2:g.109097622A>T | GRCh38 |
| NC_000008.10:g.110109851A>T , CM000670.1:g.110109851A>T | GRCh37 |
| NC_000008.9:g.110179027A>T | NCBI36 |
| NG_017161.1:g.15176A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000518632.2:c.789+9321A>T MANE Select | ENSP00000430711.2:n.789+9321A>T | |
| ENST00000311762.2:c.789+9321A>T | ENSP00000309818.2:n.789+9321A>T | |
| ENST00000518632.1:c.789+9321A>T | ENSP00000430711.1:n.789+9321A>T | |
| NM_003301.5:c.789+9321A>T | NP_003292.1:n.789+9321A>T | |
| XM_011517263.1:c.789+9321A>T | XP_011515565.1:n.789+9321A>T | |
| XM_011517263.2:c.789+9321A>T | XP_011515565.1:n.789+9321A>T | |
| NM_003301.7:c.789+9321A>T MANE Select | NP_003292.1:n.789+9321A>T |