Linked Data
dbSNP Id:
rs1240745463
gnomAD v3:
11-112016682-T-C
gnomAD v4:
11-112016682-T-C
MyVariant Identifiers:
chr11:g.112016682T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112016682T>C , CM000673.2:g.112016682T>C | GRCh38 |
| NC_000011.9:g.111887406T>C , CM000673.1:g.111887406T>C | GRCh37 |
| NC_000011.8:g.111392616T>C | NCBI36 |
| NG_033127.1:g.94540T>C | |
| NG_033127.2:g.94539T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000440460.7:c.1757-9T>C MANE Select | ENSP00000394352.3:n.1757-9T>C | |
| ENST00000440460.6:c.1757-9T>C | ENSP00000394352.3:n.1757-9T>C | |
| ENST00000526500.5:n.753-9T>C | ||
| ENST00000615255.1:c.1124-9T>C | ENSP00000480808.1:n.1124-9T>C | |
| ENST00000618522.4:n.1110-9T>C | ||
| NM_001037954.3:c.1757-9T>C | NP_001033043.1:n.1757-9T>C | |
| NM_033425.4:c.1124-9T>C | NP_219493.1:n.1124-9T>C | |
| XM_005277726.3:c.1757-9T>C | XP_005277783.1:n.1757-9T>C | |
| XM_005277727.3:c.1754-9T>C | XP_005277784.1:n.1754-9T>C | |
| XM_005277728.3:c.1124-9T>C | XP_005277785.1:n.1124-9T>C | |
| XM_011543045.1:c.875-9T>C | XP_011541347.1:n.875-9T>C | |
| XM_011543046.1:c.869-9T>C | XP_011541348.1:n.869-9T>C | |
| XM_017018466.2:c.1754-9T>C | XP_016873955.1:n.1754-9T>C | |
| XM_017018467.1:c.1754-9T>C | XP_016873956.1:n.1754-9T>C | |
| XM_017018468.1:c.875-9T>C | XP_016873957.1:n.875-9T>C | |
| XM_017018469.1:c.869-9T>C | XP_016873958.1:n.869-9T>C | |
| XM_024448742.1:c.1649-9T>C | XP_024304510.1:n.1649-9T>C | |
| XM_024448743.1:c.1646-9T>C | XP_024304511.1:n.1646-9T>C | |
| NM_001037954.4:c.1757-9T>C MANE Select | NP_001033043.1:n.1757-9T>C | |
| NM_033425.5:c.1124-9T>C | NP_219493.1:n.1124-9T>C |