HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31659727T= , CM000683.2:g.31659727T= | GRCh38 |
NC_000021.8:g.33032040T= , CM000683.1:g.33032040T= | GRCh37 |
NC_000021.7:g.31953911T= | NCBI36 |
NG_008689.1:g.5106T= , LRG_652:g.5106T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.-43T= MANE Select | ENSP00000270142.7:n.-43T= | |
ENST00000270142.10:c.-43T= | ENSP00000270142.6:n.-43T= | |
ENST00000389995.4:c.-43T= | ENSP00000374645.4:n.-43T= | |
ENST00000470944.1:n.19T= | ||
ENST00000476106.5:n.35T= | ||
NM_000454.4:c.-43T= , LRG_652t1:c.-43T= | NP_000445.1:n.-43T= | |
NM_000454.5:c.-43T= MANE Select | NP_000445.1:n.-43T= |