HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31498117A>T , CM000680.2:g.31498117A>T | GRCh38 |
NC_000018.9:g.29078080A>T , CM000680.1:g.29078080A>T | GRCh37 |
NC_000018.8:g.27332078A>T | NCBI36 |
NG_007072.3:g.4876A>T , LRG_397:g.4876A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261590.12:c.-135A>T | ENSP00000261590.8:n.-135A>T | |
NM_001943.3:c.-135A>T , LRG_397t1:c.-135A>T | NP_001934.2:n.-135A>T | |
NM_001943.4:c.-135A>T | NP_001934.2:n.-135A>T |