Linked Data
MyVariant Identifiers:
chr5:g.174151767G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.174724764G>C , CM000667.2:g.174724764G>C | GRCh38 |
| NC_000005.9:g.174151767G>C , CM000667.1:g.174151767G>C | GRCh37 |
| NC_000005.8:g.174084373G>C | NCBI36 |
| NG_008124.1:g.5193G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239243.7:c.105G>C MANE Select | ENSP00000239243.5:p.Ala35= | |
| ENST00000239243.6:c.105G>C | ENSP00000239243.5:p.Ala35= | |
| ENST00000507785.2:c.105G>C | ENSP00000427425.1:p.Ala35= | |
| NM_002449.4:c.105G>C | NP_002440.2:p.Ala35= | |
| NM_001363626.1:c.105G>C | NP_001350555.1:p.Ala35= | |
| NM_002449.5:c.105G>C MANE Select | NP_002440.2:p.Ala35= | |
| NM_001363626.2:c.105G>C | NP_001350555.1:p.Ala35= |