Linked Data
MyVariant Identifiers:
chr1:g.171621161T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171652021T>C , CM000663.2:g.171652021T>C | GRCh38 |
| NC_000001.10:g.171621161T>C , CM000663.1:g.171621161T>C | GRCh37 |
| NC_000001.9:g.169887784T>C | NCBI36 |
| NG_008859.1:g.5613A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.591A>G MANE Select | ENSP00000037502.5:p.Pro197= | |
| ENST00000638471.1:c.130+461A>G | ENSP00000491206.1:n.130+461A>G | |
| ENST00000037502.10:c.591A>G | ENSP00000037502.5:p.Pro197= | |
| ENST00000614688.1:c.591A>G | ENSP00000478680.1:p.Pro197= | |
| NM_000261.1:c.591A>G | NP_000252.1:p.Pro197= | |
| NM_000261.2:c.591A>G MANE Select | NP_000252.1:p.Pro197= |