Linked Data
MyVariant Identifiers:
chr4:g.68797752G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67932034G>C , CM000666.2:g.67932034G>C | GRCh38 |
| NC_000004.11:g.68797752G>C , CM000666.1:g.68797752G>C | GRCh37 |
| NC_000004.10:g.68480347G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000508048.6:c.279C>G MANE Select | ENSP00000426911.2:p.Ala93= | |
| ENST00000334830.11:c.288C>G | ENSP00000334611.7:p.Ala96= | |
| ENST00000396188.3:c.279C>G | ENSP00000379491.3:p.Ala93= | |
| ENST00000508048.5:c.279C>G | ENSP00000426911.2:p.Ala93= | |
| ENST00000513536.5:c.219C>G | ENSP00000427621.1:p.Ala73= | |
| NM_001114387.1:c.279C>G | NP_001107859.1:p.Ala93= | |
| NM_182606.3:c.288C>G | NP_872412.3:p.Ala96= | |
| NM_001114387.2:c.279C>G MANE Select | NP_001107859.1:p.Ala93= | |
| NM_182606.4:c.288C>G | NP_872412.3:p.Ala96= |