HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67584574A= , CM000673.2:g.67584574A= | GRCh38 |
NC_000011.9:g.67352045A= , CM000673.1:g.67352045A= | GRCh37 |
NC_000011.8:g.67108621A= | NCBI36 |
NG_012075.1:g.5980A= , LRG_723:g.5980A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.144+4A= | ENSP00000381604.1:n.144+4A= | |
ENST00000398606.10:c.144+4A= MANE Select | ENSP00000381607.3:n.144+4A= | |
ENST00000646888.1:c.38-111A= | ENSP00000494477.1:n.38-111A= | |
ENST00000398603.5:c.144+4A= | ENSP00000381604.1:n.144+4A= | |
ENST00000398606.7:c.144+4A= | ENSP00000381607.3:n.144+4A= | |
ENST00000489040.1:n.143+4A= | ||
ENST00000494593.1:n.464A= | ||
ENST00000498765.5:c.107+4A= | ||
NM_000852.3:c.144+4A= , LRG_723t1:c.144+4A= | NP_000843.1:n.144+4A= | |
NM_000852.4:c.144+4A= MANE Select | NP_000843.1:n.144+4A= |