Linked Data
dbSNP Id:
rs12141391
gnomAD v2:
1-72274473-C-A
gnomAD v3:
1-71808790-C-A
gnomAD v4:
1-71808790-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.71808790C>A , CM000663.2:g.71808790C>A | GRCh38 |
| NC_000001.10:g.72274473C>A , CM000663.1:g.72274473C>A | GRCh37 |
| NC_000001.9:g.72047061C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000357731.10:c.410-32493G>T (NEGR1) MANE Select | ENSP00000350364.4:n.410-32493G>T | |
| ENST00000306821.3:c.26-32493G>T (NEGR1) | ENSP00000305938.3:n.26-32493G>T | |
| ENST00000357731.9:c.410-32493G>T (NEGR1) | ENSP00000350364.4:n.410-32493G>T | |
| ENST00000434200.5:c.245-32493G>T (NEGR1) | ENSP00000413294.2:n.245-32493G>T | |
| ENST00000467479.1:n.407-32493G>T (NEGR1) | ||
| NM_173808.2:c.410-32493G>T (NEGR1) | NP_776169.2:n.410-32493G>T | |
| NR_046218.1:n.34-10520G>T (NEGR1-IT1) | ||
| XM_011541200.1:c.410-32493G>T (NEGR1) | XP_011539502.1:n.410-32493G>T | |
| XM_011541201.1:c.410-32493G>T (NEGR1) | XP_011539503.1:n.410-32493G>T | |
| XM_011541200.3:c.410-32493G>T (NEGR1) | XP_011539502.1:n.410-32493G>T | |
| XM_011541201.3:c.410-32493G>T (NEGR1) | XP_011539503.1:n.410-32493G>T | |
| XM_017000961.2:c.410-32493G>T (NEGR1) | XP_016856450.1:n.410-32493G>T | |
| NM_173808.3:c.410-32493G>T (NEGR1) MANE Select | NP_776169.2:n.410-32493G>T |