HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99307699A>G , CM000666.2:g.99307699A>G | GRCh38 |
NC_000004.11:g.100228856A>G , CM000666.1:g.100228856A>G | GRCh37 |
NC_000004.10:g.100447879A>G | NCBI36 |
NG_011435.1:g.18717T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305046.13:c.*141T>C MANE Select | ENSP00000306606.8:n.*141T>C | |
ENST00000305046.12:c.*141T>C | ENSP00000306606.8:n.*141T>C | |
ENST00000506651.5:c.*141T>C | ENSP00000425998.2:n.*141T>C | |
ENST00000515694.4:n.3364T>C | ||
ENST00000625860.2:c.*141T>C | ENSP00000486614.1:n.*141T>C | |
NM_000668.5:c.*141T>C | NP_000659.2:n.*141T>C | |
NM_001286650.1:c.*141T>C | NP_001273579.1:n.*141T>C | |
NM_000668.6:c.*141T>C MANE Select | NP_000659.2:n.*141T>C | |
NM_001286650.2:c.*141T>C | NP_001273579.1:n.*141T>C |