Linked Data
dbSNP Id:
rs2235649
gnomAD v2:
16-1837406-C-T
gnomAD v3:
16-1787405-C-T
gnomAD v4:
16-1787405-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1787405C>T , CM000678.2:g.1787405C>T | GRCh38 |
| NC_000016.9:g.1837406C>T , CM000678.1:g.1837406C>T | GRCh37 |
| NC_000016.8:g.1777407C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000262302.14:c.335-272C>T (NUBP2) MANE Select | ENSP00000262302.9:n.335-272C>T | |
| ENST00000262302.13:c.335-272C>T (NUBP2) | ENSP00000262302.9:n.335-272C>T | |
| ENST00000562263.5:c.155-272C>T (NUBP2) | ENSP00000456199.1:n.155-272C>T | |
| ENST00000563136.5:c.354-272C>T (NUBP2) | ENSP00000454576.1:n.354-272C>T | |
| ENST00000564227.5:c.803-272C>T (NUBP2) | ||
| ENST00000565134.5:c.335-272C>T (NUBP2) | ENSP00000454815.1:n.335-272C>T | |
| ENST00000565603.5:n.461-272C>T (NUBP2) | ||
| ENST00000565987.5:c.155-272C>T (NUBP2) | ENSP00000455896.1:n.155-272C>T | |
| ENST00000567700.5:n.974C>T (NUBP2) | ||
| ENST00000568287.5:c.599-272C>T (NUBP2) | ENSP00000454982.1:n.599-272C>T | |
| ENST00000568706.1:c.-89-272C>T (NUBP2) | ENSP00000460079.1:n.-89-272C>T | |
| ENST00000568834.5:c.136-272C>T (NUBP2) | ENSP00000456928.1:n.136-272C>T | |
| ENST00000569769.1:c.-12-5910G>A (SPSB3) | ENSP00000455098.1:n.-12-5910G>A | |
| ENST00000569898.5:c.136-272C>T (NUBP2) | ENSP00000456284.1:n.136-272C>T | |
| NM_001284501.1:c.155-272C>T (NUBP2) | NP_001271430.1:n.155-272C>T | |
| NM_001284502.1:c.-89-272C>T (NUBP2) | NP_001271431.1:n.-89-272C>T | |
| NM_012225.3:c.335-272C>T (NUBP2) | NP_036357.1:n.335-272C>T | |
| NR_104318.1:n.234-272C>T (NUBP2) | ||
| XM_005255027.1:c.155-272C>T (NUBP2) | XP_005255084.1:n.155-272C>T | |
| XM_005255028.1:c.155-272C>T (NUBP2) | XP_005255085.1:n.155-272C>T | |
| XM_005255030.1:c.-89-272C>T (NUBP2) | XP_005255087.1:n.-89-272C>T | |
| XM_011522338.1:c.164-272C>T (NUBP2) | XP_011520640.1:n.164-272C>T | |
| XM_005255027.3:c.155-272C>T (NUBP2) | XP_005255084.1:n.155-272C>T | |
| XM_011522338.2:c.164-272C>T (NUBP2) | XP_011520640.1:n.164-272C>T | |
| XM_017022831.1:c.155-272C>T (NUBP2) | XP_016878320.1:n.155-272C>T | |
| XM_017022832.2:c.197-272C>T (NUBP2) | XP_016878321.1:n.197-272C>T | |
| XM_024450135.1:c.155-272C>T (NUBP2) | XP_024305903.1:n.155-272C>T | |
| NM_012225.4:c.335-272C>T (NUBP2) MANE Select | NP_036357.1:n.335-272C>T | |
| NM_001284501.2:c.155-272C>T (NUBP2) | NP_001271430.1:n.155-272C>T | |
| NM_001284502.2:c.-89-272C>T (NUBP2) | NP_001271431.1:n.-89-272C>T | |
| NR_104318.2:n.197-272C>T (NUBP2) |