HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31659741A= , CM000683.2:g.31659741A= | GRCh38 |
NC_000021.8:g.33032054A= , CM000683.1:g.33032054A= | GRCh37 |
NC_000021.7:g.31953925A= | NCBI36 |
NG_008689.1:g.5120A= , LRG_652:g.5120A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.-29A= MANE Select | ENSP00000270142.7:n.-29A= | |
ENST00000270142.10:c.-29A= | ENSP00000270142.6:n.-29A= | |
ENST00000389995.4:c.-29A= | ENSP00000374645.4:n.-29A= | |
ENST00000470944.1:n.33A= | ||
ENST00000476106.5:n.49A= | ||
NM_000454.4:c.-29A= , LRG_652t1:c.-29A= | NP_000445.1:n.-29A= | |
NM_000454.5:c.-29A= MANE Select | NP_000445.1:n.-29A= |