HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31357184C= , CM000668.2:g.31357184C= | GRCh38 |
NC_000006.11:g.31324961C= , CM000668.1:g.31324961C= | GRCh37 |
NC_000006.10:g.31432940C= | NCBI36 |
NG_023187.1:g.5029G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000474381.2:n.1448G= | ||
ENST00000481849.6:n.1448G= | ||
ENST00000497377.6:n.1448G= | ||
ENST00000696559.1:c.-26G= | ENSP00000512717.1:n.-26G= | |
ENST00000696560.1:c.-26G= | ENSP00000512718.1:n.-26G= | |
ENST00000696561.1:c.-26G= | ENSP00000512719.1:n.-26G= | |
ENST00000696562.1:c.-26G= | ENSP00000512720.1:n.-26G= | |
ENST00000412585.6:c.-26G= | ENSP00000399168.2:n.-26G= | |
ENST00000434333.1:c.-121G= | ENSP00000405931.1:n.-121G= | |
ENST00000603274.1:n.538C= | ||
NM_005514.6:c.-26G= | NP_005505.2:n.-26G= | |
NM_005514.7:c.-26G= | NP_005505.2:n.-26G= |