Linked Data
dbSNP Id:
rs2387632
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.28342206T>A , CM000675.2:g.28342206T>A | GRCh38 |
| NC_000013.10:g.28916343T>A , CM000675.1:g.28916343T>A | GRCh37 |
| NC_000013.9:g.27814343T>A | NCBI36 |
| NG_012003.1:g.157923A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000706527.1:n.181-2906A>T | ||
| ENST00000282397.9:c.2356-2906A>T MANE Select | ENSP00000282397.4:n.2356-2906A>T | |
| ENST00000282397.8:c.2356-2906A>T | ENSP00000282397.4:n.2356-2906A>T | |
| ENST00000540678.2:c.-1404-2906A>T | ENSP00000443311.2:n.-1404-2906A>T | |
| NM_002019.4:c.2356-2906A>T MANE Select | NP_002010.2:n.2356-2906A>T | |
| XM_017020485.1:c.2356-2906A>T | XP_016875974.1:n.2356-2906A>T |