HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713781A>C , CM000681.2:g.6713781A>C | GRCh38 |
NC_000019.9:g.6713792A>C , CM000681.1:g.6713792A>C | GRCh37 |
NC_000019.8:g.6664792A>C | NCBI36 |
NG_009557.1:g.11871T>G , LRG_27:g.11871T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.650+211T>G | ENSP00000512083.1:n.650+211T>G | |
ENST00000245907.11:c.773+211T>G MANE Select | ENSP00000245907.4:n.773+211T>G | |
ENST00000245907.10:c.773+211T>G | ENSP00000245907.4:n.773+211T>G | |
ENST00000595577.1:n.277+211T>G | ||
ENST00000597442.5:n.8T>G | ||
NM_000064.3:c.773+211T>G | NP_000055.2:n.773+211T>G | |
NM_000064.4:c.773+211T>G MANE Select | NP_000055.2:n.773+211T>G |