HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6685915C= , CM000681.2:g.6685915C= | GRCh38 |
NC_000019.9:g.6685926C= , CM000681.1:g.6685926C= | GRCh37 |
NC_000019.8:g.6636926C= | NCBI36 |
NG_009557.1:g.39737G= , LRG_27:g.39737G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695651.1:n.2158+209G= | ||
ENST00000695653.1:c.1719+209G= | ENSP00000512084.1:n.1719+209G= | |
ENST00000695654.1:c.2835+209G= | ENSP00000512085.1:n.2835+209G= | |
ENST00000245907.11:c.3810+209G= MANE Select | ENSP00000245907.4:n.3810+209G= | |
ENST00000245907.10:c.3810+209G= | ENSP00000245907.4:n.3810+209G= | |
ENST00000596238.1:n.253+209G= | ||
ENST00000601008.1:c.241+831G= | ENSP00000471384.1:n.241+831G= | |
NM_000064.3:c.3810+209G= | NP_000055.2:n.3810+209G= | |
NM_000064.4:c.3810+209G= MANE Select | NP_000055.2:n.3810+209G= |