HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110602112A= , CM000672.2:g.110602112A= | GRCh38 |
NC_000010.10:g.112361870A= , CM000672.1:g.112361870A= | GRCh37 |
NC_000010.9:g.112351860A= | NCBI36 |
NG_012217.1:g.39422A= , LRG_774:g.39422A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.5272A= | ||
ENST00000685743.1:n.2747A= | ||
ENST00000686057.1:n.1390A= | ||
ENST00000689321.1:n.2002A= | ||
ENST00000689986.1:n.828A= | ||
ENST00000361804.5:c.3039A= MANE Select | ENSP00000354720.5:p.Ser1013= | |
ENST00000361804.4:c.3039A= | ENSP00000354720.4:p.Ser1013= | |
NM_005445.3:c.3039A= , LRG_774t1:c.3039A= | NP_005436.1:p.Ser1013= | |
NM_005445.4:c.3039A= MANE Select | NP_005436.1:p.Ser1013= |