Linked Data
dbSNP Id:
rs1560174866
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.17681181C>T , CM000666.2:g.17681181C>T | GRCh38 |
| NC_000004.11:g.17682804C>T , CM000666.1:g.17682804C>T | GRCh37 |
| NC_000004.10:g.17291902C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000265018.4:c.1596+7243G>A MANE Select | ENSP00000265018.3:n.1596+7243G>A | |
| ENST00000265018.3:c.1596+7243G>A | ENSP00000265018.3:n.1596+7243G>A | |
| NM_015688.1:c.1596+7243G>A | NP_056503.1:n.1596+7243G>A | |
| XM_011513834.1:c.1596+7243G>A | XP_011512136.1:n.1596+7243G>A | |
| NM_015688.2:c.1596+7243G>A MANE Select | NP_056503.1:n.1596+7243G>A |