HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94401397A= , CM000669.2:g.94401397A= | GRCh38 |
NC_000007.13:g.94030709A= , CM000669.1:g.94030709A= | GRCh37 |
NC_000007.12:g.93868645A= | NCBI36 |
NG_007405.1:g.11837A= , LRG_2:g.11837A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297268.11:c.226-170A= MANE Select | ENSP00000297268.6:n.226-170A= | |
ENST00000297268.10:c.226-170A= | ENSP00000297268.6:n.226-170A= | |
ENST00000620463.1:c.220-170A= | ENSP00000477719.1:n.220-170A= | |
NM_000089.3:c.226-170A= , LRG_2t1:c.226-170A= | NP_000080.2:n.226-170A= | |
NM_000089.4:c.226-170A= MANE Select | NP_000080.2:n.226-170A= |