HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038008C= , CM000666.2:g.52038008C= | GRCh38 |
NC_000004.11:g.52904174C= , CM000666.1:g.52904174C= | GRCh37 |
NC_000004.10:g.52598931C= | NCBI36 |
NG_008891.1:g.5312G= , LRG_204:g.5312G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.33+219G= MANE Select | ENSP00000370839.6:n.33+219G= | |
ENST00000381431.9:c.33+219G= | ENSP00000370839.5:n.33+219G= | |
ENST00000506357.5:c.19+219G= | ||
NM_000232.4:c.33+219G= , LRG_204t1:c.33+219G= | NP_000223.1:n.33+219G= | |
XM_011534403.1:c.33+219G= | XP_011532705.1:n.33+219G= | |
NM_000232.5:c.33+219G= MANE Select | NP_000223.1:n.33+219G= |