HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6714490C>A , CM000681.2:g.6714490C>A | GRCh38 |
NC_000019.9:g.6714501C>A , CM000681.1:g.6714501C>A | GRCh37 |
NC_000019.8:g.6665501C>A | NCBI36 |
NG_009557.1:g.11162G>T , LRG_27:g.11162G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.382-44G>T | ENSP00000512083.1:n.382-44G>T | |
ENST00000245907.11:c.505-44G>T MANE Select | ENSP00000245907.4:n.505-44G>T | |
ENST00000245907.10:c.505-44G>T | ENSP00000245907.4:n.505-44G>T | |
NM_000064.3:c.505-44G>T | NP_000055.2:n.505-44G>T | |
NM_000064.4:c.505-44G>T MANE Select | NP_000055.2:n.505-44G>T |