Linked Data
MyVariant Identifiers:
chr10:g.72201358C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.70441602C>G , CM000672.2:g.70441602C>G | GRCh38 |
| NC_000010.10:g.72201358C>G , CM000672.1:g.72201358C>G | GRCh37 |
| NC_000010.9:g.71871364C>G | NCBI36 |
| NG_012448.1:g.5108G>C | |
| NG_012448.2:g.11347G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000287139.8:c.66G>C MANE Select | ENSP00000287139.3:p.Ala22= | |
| ENST00000287139.7:c.66G>C | ENSP00000287139.3:p.Ala22= | |
| ENST00000414871.1:c.29-5619G>C | ENSP00000394468.1:n.29-5619G>C | |
| NM_018055.4:c.66G>C | NP_060525.3:p.Ala22= | |
| NM_001329906.1:c.-206-5619G>C | NP_001316835.1:n.-206-5619G>C | |
| XM_024448028.1:c.-207+429G>C | XP_024303796.1:n.-207+429G>C | |
| NM_018055.5:c.66G>C MANE Select | NP_060525.3:p.Ala22= | |
| NM_001329906.2:c.-206-5619G>C | NP_001316835.1:n.-206-5619G>C |