HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67584681A= , CM000673.2:g.67584681A= | GRCh38 |
NC_000011.9:g.67352152A= , CM000673.1:g.67352152A= | GRCh37 |
NC_000011.8:g.67108728A= | NCBI36 |
NG_012075.1:g.6087A= , LRG_723:g.6087A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.145-4A= | ENSP00000381604.1:n.145-4A= | |
ENST00000398606.10:c.145-4A= MANE Select | ENSP00000381607.3:n.145-4A= | |
ENST00000646888.1:c.38-4A= | ENSP00000494477.1:n.38-4A= | |
ENST00000398603.5:c.145-4A= | ENSP00000381604.1:n.145-4A= | |
ENST00000398606.7:c.145-4A= | ENSP00000381607.3:n.145-4A= | |
ENST00000489040.1:n.144-4A= | ||
ENST00000494593.1:n.571A= | ||
ENST00000498765.5:c.108-4A= | ||
NM_000852.3:c.145-4A= , LRG_723t1:c.145-4A= | NP_000843.1:n.145-4A= | |
NM_000852.4:c.145-4A= MANE Select | NP_000843.1:n.145-4A= |