HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107701046A= , CM000669.2:g.107701046A= | GRCh38 |
NC_000007.13:g.107341491A= , CM000669.1:g.107341491A= | GRCh37 |
NC_000007.12:g.107128727A= | NCBI36 |
NG_008489.1:g.45412A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000644269.2:c.1708-55A= MANE Select | ENSP00000494017.1:n.1708-55A= | |
ENST00000644846.1:c.419-55A= | ||
ENST00000265715.7:c.1708-55A= | ENSP00000265715.3:n.1708-55A= | |
ENST00000480841.5:n.557-55A= | ||
ENST00000492030.2:n.91-781A= | ||
NM_000441.1:c.1708-55A= | NP_000432.1:n.1708-55A= | |
XM_005250425.1:c.1708-55A= | XP_005250482.1:n.1708-55A= | |
XM_005250425.2:c.1708-55A= | XP_005250482.1:n.1708-55A= | |
XM_017012318.1:c.1630-55A= | XP_016867807.1:n.1630-55A= | |
NM_000441.2:c.1708-55A= MANE Select | NP_000432.1:n.1708-55A= |