Linked Data
MyVariant Identifiers:
chr7:g.94033883A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94404571A>C , CM000669.2:g.94404571A>C | GRCh38 |
| NC_000007.13:g.94033883A>C , CM000669.1:g.94033883A>C | GRCh37 |
| NC_000007.12:g.93871819A>C | NCBI36 |
| NG_007405.1:g.15011A>C , LRG_2:g.15011A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.295A>C MANE Select | ENSP00000297268.6:p.Arg99= | |
| ENST00000297268.10:c.295A>C | ENSP00000297268.6:p.Arg99= | |
| ENST00000620463.1:c.289A>C | ENSP00000477719.1:p.Arg97= | |
| NM_000089.3:c.295A>C , LRG_2t1:c.295A>C | NP_000080.2:p.Arg99= | |
| NM_000089.4:c.295A>C MANE Select | NP_000080.2:p.Arg99= |