HGVS | Genome Assembly |
---|---|
NC_000007.14:g.155812269C= , CM000669.2:g.155812269C= | GRCh38 |
NC_000007.13:g.155604963C= , CM000669.1:g.155604963C= | GRCh37 |
NC_000007.12:g.155297724C= | NCBI36 |
NG_007504.2:g.5005G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297261.7:c.-147G= MANE Select | ENSP00000297261.2:n.-147G= | |
ENST00000297261.6:c.-147G= | ENSP00000297261.2:n.-147G= | |
NM_000193.2:c.-147G= | NP_000184.1:n.-147G= | |
NM_000193.3:c.-147G= | NP_000184.1:n.-147G= | |
NM_000193.4:c.-147G= MANE Select | NP_000184.1:n.-147G= |