HGVS | Genome Assembly |
---|---|
NC_000007.14:g.155812164G= , CM000669.2:g.155812164G= | GRCh38 |
NC_000007.13:g.155604858G= , CM000669.1:g.155604858G= | GRCh37 |
NC_000007.12:g.155297619G= | NCBI36 |
NG_007504.2:g.5110C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297261.7:c.-42C= MANE Select | ENSP00000297261.2:n.-42C= | |
ENST00000297261.6:c.-42C= | ENSP00000297261.2:n.-42C= | |
NM_000193.2:c.-42C= | NP_000184.1:n.-42C= | |
NM_000193.3:c.-42C= | NP_000184.1:n.-42C= | |
NM_000193.4:c.-42C= MANE Select | NP_000184.1:n.-42C= |