HGVS | Genome Assembly |
---|---|
NC_000004.12:g.73404259T>C , CM000666.2:g.73404259T>C | GRCh38 |
NC_000004.11:g.74269976T>C , CM000666.1:g.74269976T>C | GRCh37 |
NC_000004.10:g.74488840T>C | NCBI36 |
NG_009291.1:g.5005T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000295897.8:c.-69T>C | ENSP00000295897.4:n.-69T>C | |
ENST00000441319.5:c.48-110T>C | ENSP00000392541.1:n.48-110T>C | |
ENST00000621628.4:c.-69T>C | ENSP00000480485.1:n.-69T>C | |
NM_000477.5:c.-69T>C | NP_000468.1:n.-69T>C | |
NM_000477.6:c.-69T>C | NP_000468.1:n.-69T>C |