HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6709913C>G , CM000681.2:g.6709913C>G | GRCh38 |
NC_000019.9:g.6709924C>G , CM000681.1:g.6709924C>G | GRCh37 |
NC_000019.8:g.6660924C>G | NCBI36 |
NG_009557.1:g.15739G>C , LRG_27:g.15739G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.1564-71G>C | ENSP00000512083.1:n.1564-71G>C | |
ENST00000695654.1:c.811-71G>C | ENSP00000512085.1:n.811-71G>C | |
ENST00000695655.1:c.592-35G>C | ENSP00000512086.1:n.592-35G>C | |
ENST00000695692.1:n.1051-71G>C | ||
ENST00000245907.11:c.1687-71G>C MANE Select | ENSP00000245907.4:n.1687-71G>C | |
ENST00000245907.10:c.1687-71G>C | ENSP00000245907.4:n.1687-71G>C | |
ENST00000600763.1:n.320-71G>C | ||
NM_000064.3:c.1687-71G>C | NP_000055.2:n.1687-71G>C | |
NM_000064.4:c.1687-71G>C MANE Select | NP_000055.2:n.1687-71G>C |