HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47335218G= , CM000673.2:g.47335218G= | GRCh38 |
NC_000011.9:g.47356769G= , CM000673.1:g.47356769G= | GRCh37 |
NC_000011.8:g.47313345G= | NCBI36 |
NG_007667.1:g.22485C= , LRG_386:g.22485C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000545968.6:c.2738-9C= MANE Select | ENSP00000442795.1:n.2738-9C= | |
ENST00000256993.8:c.2738-9C= | ENSP00000256993.5:n.2738-9C= | |
ENST00000399249.6:c.2738-9C= | ENSP00000382193.2:n.2738-9C= | |
ENST00000545968.5:c.2738-9C= | ENSP00000442795.1:n.2738-9C= | |
NM_000256.3:c.2738-9C= , LRG_386t1:c.2738-9C= MANE Select | NP_000247.2:n.2738-9C= | |
XM_011520117.1:c.2720-9C= | XP_011518419.1:n.2720-9C= | |
XM_011520118.1:c.2657-9C= | XP_011518420.1:n.2657-9C= |