Linked Data
dbSNP Id:
rs1555092376
gnomAD v3:
11-71084539-A-G
gnomAD v4:
11-71084539-A-G
MyVariant Identifiers:
chr11:g.71084539A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.71084539A>G , CM000673.2:g.71084539A>G | GRCh38 |
| NG_042866.1:g.145258T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000601538.6:c.912+7883T>C MANE Select | ENSP00000469689.2:n.912+7883T>C | |
| ENST00000458632.2:c.320+7883T>C | ||
| ENST00000601538.5:c.912+7883T>C | ENSP00000469689.2:n.912+7883T>C | |
| ENST00000608988.5:c.*475+7883T>C | ENSP00000476264.2:n.*475+7883T>C | |
| ENST00000618363.4:c.56+7883T>C | ||
| NM_012309.4:c.912+7883T>C | NP_036441.2:n.912+7883T>C | |
| XM_005277930.2:c.912+7883T>C | XP_005277987.1:n.912+7883T>C | |
| XM_006718478.2:c.912+7883T>C | XP_006718541.1:n.912+7883T>C | |
| XM_011544854.1:c.912+7883T>C | XP_011543156.1:n.912+7883T>C | |
| XM_011544855.1:c.912+7883T>C | XP_011543157.1:n.912+7883T>C | |
| XM_011544856.1:c.912+7883T>C | XP_011543158.1:n.912+7883T>C | |
| XM_011544857.1:c.912+7883T>C | XP_011543159.1:n.912+7883T>C | |
| XM_011544858.1:c.912+7883T>C | XP_011543160.1:n.912+7883T>C | |
| XM_017017387.1:c.912+7883T>C | XP_016872876.1:n.912+7883T>C | |
| XM_017017388.1:c.912+7883T>C | XP_016872877.1:n.912+7883T>C | |
| XM_017017389.1:c.912+7883T>C | XP_016872878.1:n.912+7883T>C | |
| NM_012309.5:c.912+7883T>C MANE Select | NP_036441.2:n.912+7883T>C |