HGVS | Genome Assembly |
---|---|
NC_000004.12:g.46993535G= , CM000666.2:g.46993535G= | GRCh38 |
NC_000004.11:g.46995552G= , CM000666.1:g.46995552G= | GRCh37 |
NC_000004.10:g.46690309G= | NCBI36 |
NG_011809.1:g.5029C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264318.4:c.-111C= MANE Select | ENSP00000264318.3:n.-111C= | |
ENST00000264318.3:c.-111C= | ENSP00000264318.3:n.-111C= | |
ENST00000502874.1:c.-111C= | ENSP00000424386.1:n.-111C= | |
ENST00000509316.1:n.14C= | ||
NM_000809.3:c.-111C= | NP_000800.2:n.-111C= | |
XM_011513677.1:c.-111C= | XP_011511979.1:n.-111C= | |
NM_000809.4:c.-111C= MANE Select | NP_000800.2:n.-111C= | |
NM_001204266.2:c.-100C= | NP_001191195.1:n.-100C= | |
NM_001204267.2:c.-100C= | NP_001191196.1:n.-100C= |