Linked Data
dbSNP Id:
rs2126583684
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186195936T>G , CM000666.2:g.186195936T>G | GRCh38 |
| NC_000004.11:g.187117090T>G , CM000666.1:g.187117090T>G | GRCh37 |
| NC_000004.10:g.187354084T>G | NCBI36 |
| NG_007965.1:g.9417T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.328-67T>G MANE Select | ENSP00000368079.4:n.328-67T>G | |
| ENST00000378802.4:c.328-67T>G | ENSP00000368079.4:n.328-67T>G | |
| NM_207352.3:c.328-67T>G | NP_997235.3:n.328-67T>G | |
| XM_005262935.2:c.328-67T>G | XP_005262992.1:n.328-67T>G | |
| XM_006714184.2:c.18-1004T>G | XP_006714247.1:n.18-1004T>G | |
| XM_005262935.4:c.328-67T>G | XP_005262992.1:n.328-67T>G | |
| XM_017008037.1:c.18-1004T>G | XP_016863526.1:n.18-1004T>G | |
| NM_207352.4:c.328-67T>G MANE Select | NP_997235.3:n.328-67T>G |