Linked Data
ClinVar Variation Id:
2847264
ClinVar RCV Id:
RCV003690706
MyVariant Identifiers:
chrX:g.153171542C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153906088C>T , CM000685.2:g.153906088C>T | GRCh38 |
| NC_000023.10:g.153171542C>T , CM000685.1:g.153171542C>T | GRCh37 |
| NC_000023.9:g.152824736C>T | NCBI36 |
| NG_008687.1:g.6115C>T | |
| NG_009645.3:g.8136G>A | |
| NG_013220.1:g.25173G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646375.2:c.582C>T (AVPR2) MANE Select | ENSP00000496396.1:p.Ala194= | |
| ENST00000434679.6:c.95C>T (AVPR2) | ENSP00000393397.1:p.Pro32Leu | |
| ENST00000642393.1:c.97+2982G>A | ||
| ENST00000646191.1:c.97+2982G>A | ||
| ENST00000646375.1:c.582C>T (AVPR2) | ENSP00000496396.1:p.Ala194= | |
| ENST00000337474.5:c.582C>T (AVPR2) | ENSP00000338072.5:p.Ala194= | |
| ENST00000358927.6:c.582C>T (AVPR2) | ENSP00000351805.2:p.Ala194= | |
| ENST00000370049.1:c.582C>T (AVPR2) | ENSP00000359066.1:p.Ala194= | |
| ENST00000430697.1:c.582C>T (AVPR2) | ENSP00000393513.1:p.Ala194= | |
| ENST00000434679.5:c.95C>T (AVPR2) | ENSP00000393397.1:p.Pro32Leu | |
| ENST00000464967.5:n.154+2982G>A (L1CAM) | ||
| NM_000054.4:c.582C>T (AVPR2) | NP_000045.1:p.Ala194= | |
| NM_001146151.1:c.582C>T (AVPR2) | NP_001139623.1:p.Ala194= | |
| NR_027419.1:n.629C>T (AVPR2) | ||
| XM_006724828.2:c.582C>T (AVPR2) | XP_006724891.1:p.Ala194= | |
| NM_000054.5:c.582C>T (AVPR2) | NP_000045.1:p.Ala194= | |
| NM_001146151.2:c.582C>T (AVPR2) | NP_001139623.1:p.Ala194= | |
| XM_006724828.3:c.582C>T (AVPR2) | XP_006724891.1:p.Ala194= | |
| NM_000054.6:c.582C>T (AVPR2) | NP_000045.1:p.Ala194= | |
| NM_001146151.3:c.582C>T (AVPR2) | NP_001139623.1:p.Ala194= | |
| NR_027419.2:n.535C>T (AVPR2) | ||
| NM_000054.7:c.582C>T (AVPR2) MANE Select | NP_000045.1:p.Ala194= |