HGVS | Genome Assembly |
---|---|
NC_000006.12:g.6224679T= , CM000668.2:g.6224679T= | GRCh38 |
NC_000006.11:g.6224912T= , CM000668.1:g.6224912T= | GRCh37 |
NC_000006.10:g.6169911T= | NCBI36 |
NG_008107.1:g.101013A= , LRG_549:g.101013A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264870.8:c.973+7A= MANE Select | ENSP00000264870.3:n.973+7A= | |
ENST00000264870.7:c.973+7A= | ENSP00000264870.3:n.973+7A= | |
ENST00000445223.1:c.123+7A= | ||
NM_000129.3:c.973+7A= , LRG_549t1:c.973+7A= | NP_000120.2:n.973+7A= | |
XM_006715010.2:c.973+7A= | XP_006715073.1:n.973+7A= | |
XM_011514342.1:c.1135+7A= | XP_011512644.1:n.1135+7A= | |
NM_000129.4:c.973+7A= MANE Select | NP_000120.2:n.973+7A= |