Linked Data
ClinVar Variation Id:
10851
ClinVar RCV Id:
RCV000011598
dbSNP Id:
rs104894758
PubMed:
PMID:10770218
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153905819T>G , CM000685.2:g.153905819T>G | GRCh38 |
| NC_000023.10:g.153171273T>G , CM000685.1:g.153171273T>G | GRCh37 |
| NC_000023.9:g.152824467T>G | NCBI36 |
| NG_008687.1:g.5846T>G | |
| NG_009645.3:g.8405A>C | |
| NG_013220.1:g.25442A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000646375.2:c.313T>G (AVPR2) MANE Select | ENSP00000496396.1:p.Phe105Val | |
| ENST00000434679.6:c.26-200T>G (AVPR2) | ENSP00000393397.1:n.26-200T>G | |
| ENST00000642393.1:c.97+3251A>C | ||
| ENST00000646191.1:c.97+3251A>C | ||
| ENST00000646375.1:c.313T>G (AVPR2) | ENSP00000496396.1:p.Phe105Val | |
| ENST00000337474.5:c.313T>G (AVPR2) | ENSP00000338072.5:p.Phe105Val | |
| ENST00000358927.6:c.313T>G (AVPR2) | ENSP00000351805.2:p.Phe105Val | |
| ENST00000370049.1:c.313T>G (AVPR2) | ENSP00000359066.1:p.Phe105Val | |
| ENST00000430697.1:c.313T>G (AVPR2) | ENSP00000393513.1:p.Phe105Val | |
| ENST00000434679.5:c.26-200T>G (AVPR2) | ENSP00000393397.1:n.26-200T>G | |
| ENST00000464967.5:n.154+3251A>C (L1CAM) | ||
| NM_000054.4:c.313T>G (AVPR2) | NP_000045.1:p.Phe105Val | |
| NM_001146151.1:c.313T>G (AVPR2) | NP_001139623.1:p.Phe105Val | |
| NR_027419.1:n.560-200T>G (AVPR2) | ||
| XM_006724828.2:c.313T>G (AVPR2) | XP_006724891.1:p.Phe105Val | |
| NM_000054.5:c.313T>G (AVPR2) | NP_000045.1:p.Phe105Val | |
| NM_001146151.2:c.313T>G (AVPR2) | NP_001139623.1:p.Phe105Val | |
| XM_006724828.3:c.313T>G (AVPR2) | XP_006724891.1:p.Phe105Val | |
| NM_000054.6:c.313T>G (AVPR2) | NP_000045.1:p.Phe105Val | |
| NM_001146151.3:c.313T>G (AVPR2) | NP_001139623.1:p.Phe105Val | |
| NR_027419.2:n.466-200T>G (AVPR2) | ||
| NM_000054.7:c.313T>G (AVPR2) MANE Select | NP_000045.1:p.Phe105Val |