Linked Data
MyVariant Identifiers:
chr8:g.118847758T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117835519T>G , CM000670.2:g.117835519T>G | GRCh38 |
| NC_000008.10:g.118847758T>G , CM000670.1:g.118847758T>G | GRCh37 |
| NC_000008.9:g.118916939T>G | NCBI36 |
| NG_007455.2:g.281301A>C , LRG_493:g.281301A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.556A>C | ||
| ENST00000378204.7:c.1089A>C MANE Select | ENSP00000367446.3:p.Gly363= | |
| ENST00000436216.2:c.457A>C | ||
| ENST00000378204.6:c.1089A>C | ENSP00000367446.2:p.Gly363= | |
| ENST00000436216.1:c.457A>C | ||
| ENST00000437196.1:c.106A>C | ENSP00000407299.1:p.Met36Leu | |
| NM_000127.2:c.1089A>C , LRG_493t1:c.1089A>C | NP_000118.2:p.Gly363= | |
| NM_000127.3:c.1089A>C MANE Select | NP_000118.2:p.Gly363= |