HGVS | Genome Assembly |
---|---|
NC_000001.11:g.196995709T= , CM000663.2:g.196995709T= | GRCh38 |
NC_000001.10:g.196964839T= , CM000663.1:g.196964839T= | GRCh37 |
NC_000001.9:g.195231462T= | NCBI36 |
NG_016365.1:g.23173T= , LRG_227:g.23173T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699466.1:c.353-8T= | ENSP00000514393.1:n.353-8T= | |
ENST00000699467.1:n.677-8T= | ||
ENST00000699468.1:c.-24-405T= | ENSP00000514394.1:n.-24-405T= | |
ENST00000256785.5:c.608-8T= MANE Select | ENSP00000256785.4:n.608-8T= | |
ENST00000256785.4:c.608-8T= | ENSP00000256785.4:n.608-8T= | |
NM_030787.3:c.608-8T= , LRG_227t1:c.608-8T= | NP_110414.1:n.608-8T= | |
XM_011510020.1:c.617-8T= | XP_011508322.1:n.617-8T= | |
XM_011510020.2:c.617-8T= | XP_011508322.1:n.617-8T= | |
NM_030787.4:c.608-8T= MANE Select | NP_110414.1:n.608-8T= |