HGVS | Genome Assembly |
---|---|
NC_000002.12:g.112830772A= , CM000664.2:g.112830772A= | GRCh38 |
NC_000002.11:g.113588349A= , CM000664.1:g.113588349A= | GRCh37 |
NC_000002.10:g.113304820A= | NCBI36 |
NG_008851.1:g.11008T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263341.7:c.598-199T= MANE Select | ENSP00000263341.2:n.598-199T= | |
ENST00000263341.6:c.598-199T= | ENSP00000263341.2:n.598-199T= | |
ENST00000491056.5:n.1405-199T= | ||
NM_000576.2:c.598-199T= | NP_000567.1:n.598-199T= | |
XM_006712496.1:c.364-199T= | XP_006712559.1:n.364-199T= | |
XM_017003988.2:c.505-199T= | XP_016859477.1:n.505-199T= | |
NM_000576.3:c.598-199T= MANE Select | NP_000567.1:n.598-199T= |