Linked Data
MyVariant Identifiers:
chr1:g.171621632G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171652492G>C , CM000663.2:g.171652492G>C | GRCh38 |
| NC_000001.10:g.171621632G>C , CM000663.1:g.171621632G>C | GRCh37 |
| NC_000001.9:g.169888255G>C | NCBI36 |
| NG_008859.1:g.5142C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.120C>G MANE Select | ENSP00000037502.5:p.Ala40= | |
| ENST00000638471.1:c.120C>G | ENSP00000491206.1:p.Ala40= | |
| ENST00000037502.10:c.120C>G | ENSP00000037502.5:p.Ala40= | |
| ENST00000614688.1:c.120C>G | ENSP00000478680.1:p.Ala40= | |
| NM_000261.1:c.120C>G | NP_000252.1:p.Ala40= | |
| NM_000261.2:c.120C>G MANE Select | NP_000252.1:p.Ala40= |