HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713351G= , CM000681.2:g.6713351G= | GRCh38 |
NC_000019.9:g.6713362G= , CM000681.1:g.6713362G= | GRCh37 |
NC_000019.8:g.6664362G= | NCBI36 |
NG_009557.1:g.12301C= , LRG_27:g.12301C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.754-36C= | ENSP00000512083.1:n.754-36C= | |
ENST00000695692.1:n.201-36C= | ||
ENST00000245907.11:c.877-36C= MANE Select | ENSP00000245907.4:n.877-36C= | |
ENST00000245907.10:c.877-36C= | ENSP00000245907.4:n.877-36C= | |
ENST00000595577.1:n.381-36C= | ||
ENST00000597442.5:n.127-36C= | ||
NM_000064.3:c.877-36C= | NP_000055.2:n.877-36C= | |
NM_000064.4:c.877-36C= MANE Select | NP_000055.2:n.877-36C= |