HGVS | Genome Assembly |
---|---|
NC_000003.12:g.126510622C= , CM000665.2:g.126510622C= | GRCh38 |
NC_000003.11:g.126229465C= , CM000665.1:g.126229465C= | GRCh37 |
NC_000003.10:g.127712155C= | NCBI36 |
NG_016286.1:g.12130G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000290868.7:c.257+42G= MANE Select | ENSP00000290868.2:n.257+42G= | |
ENST00000290868.6:c.257+42G= | ENSP00000290868.2:n.257+42G= | |
ENST00000383579.3:c.257+42G= | ENSP00000373073.3:n.257+42G= | |
NM_001165974.1:c.257+42G= | NP_001159446.1:n.257+42G= | |
NM_144639.2:c.257+42G= | NP_653240.1:n.257+42G= | |
NM_144639.3:c.257+42G= MANE Select | NP_653240.1:n.257+42G= | |
NM_001165974.2:c.257+42G= | NP_001159446.1:n.257+42G= |