HGVS | Genome Assembly |
---|---|
NC_000010.11:g.49368594C= , CM000672.2:g.49368594C= | GRCh38 |
NC_000010.10:g.50576639C= , CM000672.1:g.50576639C= | GRCh37 |
NC_000010.9:g.50246645C= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000374139.8:c.527-2213G= MANE Select | ENSP00000363254.1:n.527-2213G= | |
ENST00000374139.6:c.527-2213G= | ENSP00000363254.1:n.527-2213G= | |
ENST00000434016.2:c.527-2213G= | ENSP00000401653.2:n.527-2213G= | |
NM_001276451.1:c.527-2213G= | NP_001263380.1:n.527-2213G= | |
XM_011540089.1:c.632-2213G= | XP_011538391.1:n.632-2213G= | |
XM_011540090.1:c.212-2213G= | XP_011538392.1:n.212-2213G= | |
XM_011540089.3:c.632-2213G= | XP_011538391.1:n.632-2213G= | |
NM_001276451.2:c.527-2213G= MANE Select | NP_001263380.1:n.527-2213G= |