HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154957052A= , CM000685.2:g.154957052A= | GRCh38 |
NC_000023.10:g.154185327A= , CM000685.1:g.154185327A= | GRCh37 |
NC_000023.9:g.153838521A= | NCBI36 |
NG_011403.1:g.70672T= | |
NG_011403.2:g.70672T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.1657T= MANE Select | ENSP00000353393.4:p.Ser553= | |
ENST00000647125.1:c.*1533T= | ENSP00000496062.1:n.*1533T= | |
ENST00000360256.8:c.1657T= | ENSP00000353393.4:p.Ser553= | |
NM_000132.3:c.1657T= | NP_000123.1:p.Ser553= | |
XM_011531126.1:c.1552T= | XP_011529428.1:p.Ser518= | |
NM_000132.4:c.1657T= MANE Select | NP_000123.1:p.Ser553= |