HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99307664A>T , CM000666.2:g.99307664A>T | GRCh38 |
NC_000004.11:g.100228821A>T , CM000666.1:g.100228821A>T | GRCh37 |
NC_000004.10:g.100447844A>T | NCBI36 |
NG_011435.1:g.18752T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000305046.13:c.*176T>A MANE Select | ENSP00000306606.8:n.*176T>A | |
ENST00000305046.12:c.*176T>A | ENSP00000306606.8:n.*176T>A | |
ENST00000506651.5:c.*176T>A | ENSP00000425998.2:n.*176T>A | |
ENST00000515694.4:n.3399T>A | ||
ENST00000625860.2:c.*176T>A | ENSP00000486614.1:n.*176T>A | |
NM_000668.5:c.*176T>A | NP_000659.2:n.*176T>A | |
NM_001286650.1:c.*176T>A | NP_001273579.1:n.*176T>A | |
NM_000668.6:c.*176T>A MANE Select | NP_000659.2:n.*176T>A | |
NM_001286650.2:c.*176T>A | NP_001273579.1:n.*176T>A |