HGVS | Genome Assembly |
---|---|
NC_000002.12:g.112831127T= , CM000664.2:g.112831127T= | GRCh38 |
NC_000002.11:g.113588704T= , CM000664.1:g.113588704T= | GRCh37 |
NC_000002.10:g.113305175T= | NCBI36 |
NG_008851.1:g.10653A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263341.7:c.597+165A= MANE Select | ENSP00000263341.2:n.597+165A= | |
ENST00000263341.6:c.597+165A= | ENSP00000263341.2:n.597+165A= | |
ENST00000491056.5:n.1404+165A= | ||
NM_000576.2:c.597+165A= | NP_000567.1:n.597+165A= | |
XM_006712496.1:c.363+165A= | XP_006712559.1:n.363+165A= | |
XM_017003988.2:c.504+165A= | XP_016859477.1:n.504+165A= | |
NM_000576.3:c.597+165A= MANE Select | NP_000567.1:n.597+165A= |