HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31667330G>C , CM000683.2:g.31667330G>C | GRCh38 |
NC_000021.8:g.33039643G>C , CM000683.1:g.33039643G>C | GRCh37 |
NC_000021.7:g.31961514G>C | NCBI36 |
NG_008689.1:g.12709G>C , LRG_652:g.12709G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.312G>C MANE Select | ENSP00000270142.7:p.Val104= | |
ENST00000270142.10:c.312G>C | ENSP00000270142.6:p.Val104= | |
ENST00000389995.4:c.255G>C | ENSP00000374645.4:p.Val85= | |
ENST00000470944.1:n.1240G>C | ||
ENST00000476106.5:n.575G>C | ||
NM_000454.4:c.312G>C , LRG_652t1:c.312G>C | NP_000445.1:p.Val104= | |
NM_000454.5:c.312G>C MANE Select | NP_000445.1:p.Val104= |