HGVS | Genome Assembly |
---|---|
NC_000009.12:g.98541565G>A , CM000671.2:g.98541565G>A | GRCh38 |
NC_000009.11:g.101303847G>A , CM000671.1:g.101303847G>A | GRCh37 |
NC_000009.10:g.100343668G>A | NCBI36 |
NG_016426.1:g.172633C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259455.4:c.630+308C>T MANE Select | ENSP00000259455.2:n.630+308C>T | |
ENST00000637410.1:n.408+308C>T | ||
ENST00000259455.3:c.630+308C>T | ENSP00000259455.2:n.630+308C>T | |
ENST00000477471.1:n.417+308C>T | ||
ENST00000634227.1:n.404+308C>T | ||
NM_005458.7:c.630+308C>T | NP_005449.5:n.630+308C>T | |
XM_017015331.2:c.336+308C>T | XP_016870820.1:n.336+308C>T | |
NM_005458.8:c.630+308C>T MANE Select | NP_005449.5:n.630+308C>T |