HGVS | Genome Assembly |
---|---|
NC_000010.11:g.62518969A>T , CM000672.2:g.62518969A>T | GRCh38 |
NC_000010.10:g.64278728A>T , CM000672.1:g.64278728A>T | GRCh37 |
NC_000010.9:g.63948734A>T | NCBI36 |
NG_021209.1:g.149813A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647733.1:c.981+59172A>T | ENSP00000502188.1:n.981+59172A>T | |
ENST00000410046.7:c.981+59172A>T | ENSP00000387091.3:n.981+59172A>T | |
NM_199451.2:c.981+59172A>T | NP_955523.1:n.981+59172A>T | |
XM_017015937.2:c.982-25240A>T | XP_016871426.1:n.982-25240A>T | |
NM_199451.3:c.981+59172A>T | NP_955523.1:n.981+59172A>T |