HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31659803G>C , CM000683.2:g.31659803G>C | GRCh38 |
NC_000021.8:g.33032116G>C , CM000683.1:g.33032116G>C | GRCh37 |
NC_000021.7:g.31953987G>C | NCBI36 |
NG_008689.1:g.5182G>C , LRG_652:g.5182G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.34G>C MANE Select | ENSP00000270142.7:p.Asp12His | |
ENST00000270142.10:c.34G>C | ENSP00000270142.6:p.Asp12His | |
ENST00000389995.4:c.15+19G>C | ENSP00000374645.4:n.15+19G>C | |
ENST00000470944.1:n.95G>C | ||
ENST00000476106.5:n.111G>C | ||
NM_000454.4:c.34G>C , LRG_652t1:c.34G>C | NP_000445.1:p.Asp12His | |
NM_000454.5:c.34G>C MANE Select | NP_000445.1:p.Asp12His |