HGVS | Genome Assembly |
---|---|
NC_000011.10:g.58863970A>T , CM000673.2:g.58863970A>T | GRCh38 |
NC_000011.9:g.58631443A>T , CM000673.1:g.58631443A>T | GRCh37 |
NC_000011.8:g.58388019A>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000533636.1:n.61-25602T>A | ||
XM_011544809.3:c.-136-19446T>A | XP_011543111.1:n.-136-19446T>A | |
XM_017017337.2:c.-269-19446T>A | XP_016872826.1:n.-269-19446T>A | |
XM_017017338.2:c.-40-24318T>A | XP_016872827.1:n.-40-24318T>A | |
XM_024448394.1:c.-131-19446T>A | XP_024304162.1:n.-131-19446T>A | |
XM_024448395.1:c.-131-19446T>A | XP_024304163.1:n.-131-19446T>A |