HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110578686T= , CM000672.2:g.110578686T= | GRCh38 |
NC_000010.10:g.112338444T= , CM000672.1:g.112338444T= | GRCh37 |
NC_000010.9:g.112328434T= | NCBI36 |
NG_012217.1:g.15996T= , LRG_774:g.15996T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.542T= | ||
ENST00000687823.1:n.323T= | ||
ENST00000689932.1:n.2472T= | ||
ENST00000691297.1:n.542T= | ||
ENST00000691527.1:n.1212T= | ||
ENST00000692792.1:n.528T= | ||
ENST00000361804.5:c.409T= MANE Select | ENSP00000354720.5:p.Tyr137= | |
ENST00000361804.4:c.409T= | ENSP00000354720.4:p.Tyr137= | |
ENST00000462899.1:n.555T= | ||
NM_005445.3:c.409T= , LRG_774t1:c.409T= | NP_005436.1:p.Tyr137= | |
NM_005445.4:c.409T= MANE Select | NP_005436.1:p.Tyr137= |