HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189003259A>T , CM000664.2:g.189003259A>T | GRCh38 |
NC_000002.11:g.189867985A>T , CM000664.1:g.189867985A>T | GRCh37 |
NC_000002.10:g.189576230A>T | NCBI36 |
NG_007404.1:g.33887A>T , LRG_3:g.33887A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.2455-152A>T | ENSP00000415346.2:n.2455-152A>T | |
ENST00000304636.9:c.2554-152A>T MANE Select | ENSP00000304408.4:n.2554-152A>T | |
ENST00000304636.7:c.2554-152A>T | ENSP00000304408.3:n.2554-152A>T | |
ENST00000317840.9:c.2527+223A>T | ENSP00000315243.6:n.2527+223A>T | |
NM_000090.3:c.2554-152A>T , LRG_3t1:c.2554-152A>T | NP_000081.1:n.2554-152A>T | |
NM_000090.4:c.2554-152A>T MANE Select | NP_000081.2:n.2554-152A>T |