HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7527092T= , CM000681.2:g.7527092T= | GRCh38 |
NC_000019.9:g.7591978T= , CM000681.1:g.7591978T= | GRCh37 |
NC_000019.8:g.7497978T= | NCBI36 |
NG_015806.1:g.9483T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264079.11:c.571+166T= MANE Select | ENSP00000264079.5:n.571+166T= | |
ENST00000264079.10:c.571+166T= | ENSP00000264079.5:n.571+166T= | |
ENST00000394321.9:n.651+166T= | ||
ENST00000596008.1:n.699T= | ||
ENST00000598406.1:n.392+166T= | ||
ENST00000601003.1:c.571+166T= | ENSP00000469074.1:n.571+166T= | |
NM_020533.2:c.571+166T= | NP_065394.1:n.571+166T= | |
NM_020533.3:c.571+166T= MANE Select | NP_065394.1:n.571+166T= |