HGVS | Genome Assembly |
---|---|
NC_000001.11:g.84100852A= , CM000663.2:g.84100852A= | GRCh38 |
NC_000001.10:g.84566535A= , CM000663.1:g.84566535A= | GRCh37 |
NC_000001.9:g.84339123A= | NCBI36 |
NG_029728.1:g.27791A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370688.7:c.46+22481A= | ENSP00000359722.3:n.46+22481A= | |
ENST00000370689.6:c.46+22481A= | ENSP00000359723.2:n.46+22481A= | |
NM_002731.3:c.46+22481A= | NP_002722.1:n.46+22481A= | |
NM_207578.2:c.46+22481A= | NP_997461.1:n.46+22481A= | |
XM_011541764.1:c.46+22481A= | XP_011540066.1:n.46+22481A= | |
XM_017001713.2:c.46+22481A= | XP_016857202.1:n.46+22481A= | |
NM_001375576.1:c.46+22481A= | NP_001362505.1:n.46+22481A= | |
NM_207578.3:c.46+22481A= | NP_997461.1:n.46+22481A= | |
NM_002731.4:c.46+22481A= | NP_002722.1:n.46+22481A= |