HGVS | Genome Assembly |
---|---|
NC_000023.11:g.22032973C= , CM000685.2:g.22032973C= | GRCh38 |
NC_000023.10:g.22051091C= , CM000685.1:g.22051091C= | GRCh37 |
NC_000023.9:g.21961012C= | NCBI36 |
NG_007563.2:g.5171C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000475778.2:n.394C= | ||
ENST00000683214.1:n.394C= | ||
ENST00000684143.1:c.-33C= | ENSP00000508264.1:n.-33C= | |
ENST00000379374.5:c.-33C= MANE Select | ENSP00000368682.4:n.-33C= | |
ENST00000379374.4:c.-33C= | ENSP00000368682.4:n.-33C= | |
NM_000444.5:c.-33C= | NP_000435.3:n.-33C= | |
NM_001282754.1:c.-33C= | NP_001269683.1:n.-33C= | |
XM_011545535.1:c.-33C= | XP_011543837.1:n.-33C= | |
XR_001755695.1:n.647C= | ||
NM_000444.6:c.-33C= MANE Select | NP_000435.3:n.-33C= | |
NM_001282754.2:c.-33C= | NP_001269683.1:n.-33C= |