MyVariant.info:
GRCh37
chr11:g.67353580G>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67586109G>C , CM000673.2:g.67586109G>C | GRCh38 |
| NC_000011.9:g.67353580G>C , CM000673.1:g.67353580G>C | GRCh37 |
| NC_000011.8:g.67110156G>C | NCBI36 |
| NG_012075.1:g.7515G>C , LRG_723:g.7515G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.337-280G>C | ENSP00000381604.1:n.337-280G>C | |
| ENST00000398606.10:c.342G>C MANE Select | ENSP00000381607.3:p.Ala114= | |
| ENST00000646888.1:c.*58G>C | ENSP00000494477.1:n.*58G>C | |
| ENST00000398603.5:c.337-280G>C | ENSP00000381604.1:n.337-280G>C | |
| ENST00000398606.7:c.342G>C | ENSP00000381607.3:p.Ala114= | |
| ENST00000467591.1:n.453G>C | ||
| ENST00000494593.1:n.1137G>C | ||
| ENST00000495996.1:c.6G>C | ENSP00000484686.1:p.Ala2= | |
| ENST00000498765.5:c.405G>C | ||
| NM_000852.3:c.342G>C , LRG_723t1:c.342G>C | NP_000843.1:p.Ala114= | |
| NM_000852.4:c.342G>C MANE Select | NP_000843.1:p.Ala114= |