HGVS | Genome Assembly |
---|---|
NC_000002.12:g.188993478A= , CM000664.2:g.188993478A= | GRCh38 |
NC_000002.11:g.189858204A= , CM000664.1:g.189858204A= | GRCh37 |
NC_000002.10:g.189566449A= | NCBI36 |
NG_007404.1:g.24106A= , LRG_3:g.24106A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000450867.2:c.1050+538A= | ENSP00000415346.2:n.1050+538A= | |
ENST00000304636.9:c.1149+19A= MANE Select | ENSP00000304408.4:n.1149+19A= | |
ENST00000304636.7:c.1149+19A= | ENSP00000304408.3:n.1149+19A= | |
ENST00000317840.9:c.1149+19A= | ENSP00000315243.6:n.1149+19A= | |
ENST00000450867.1:c.148+538A= | ||
NM_000090.3:c.1149+19A= , LRG_3t1:c.1149+19A= | NP_000081.1:n.1149+19A= | |
NM_000090.4:c.1149+19A= MANE Select | NP_000081.2:n.1149+19A= |