HGVS | Genome Assembly |
---|---|
NC_000009.12:g.21998114C>T , CM000671.2:g.21998114C>T | GRCh38 |
NC_000009.11:g.21998113C>T , CM000671.1:g.21998113C>T | GRCh37 |
NC_000009.10:g.21988113C>T | NCBI36 |
NG_007485.1:g.1378G>A , LRG_11:g.1378G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000404796.3:c.348-31319C>T | ENSP00000385916.2:n.348-31319C>T | |
ENST00000404796.2:c.348-31319C>T | ENSP00000385916.2:n.348-31319C>T | |
NR_003529.3:n.371+2953C>T | ||
NR_047532.1:n.371+2953C>T | ||
NR_047533.1:n.371+2953C>T | ||
NR_047534.1:n.371+2953C>T | ||
NR_047535.1:n.371+2953C>T | ||
NR_047536.1:n.371+2953C>T | ||
NR_047537.1:n.371+2953C>T | ||
NR_047538.1:n.371+2953C>T | ||
NR_047539.1:n.371+2953C>T | ||
NR_047540.1:n.371+2953C>T | ||
NR_047541.1:n.371+2953C>T | ||
NR_047542.1:n.371+2953C>T | ||
NR_047543.1:n.371+2953C>T | ||
NR_120536.1:n.371+2953C>T |