HGVS | Genome Assembly |
---|---|
NC_000001.11:g.67009085C>T , CM000663.2:g.67009085C>T | GRCh38 |
NC_000001.10:g.67474768C>T , CM000663.1:g.67474768C>T | GRCh37 |
NC_000001.9:g.67247356C>T | NCBI36 |
NG_012933.1:g.50313G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000235345.6:c.959G>A MANE Select | ENSP00000235345.5:p.Ser320Asn | |
ENST00000235345.5:c.959G>A | ENSP00000235345.5:p.Ser320Asn | |
NM_015139.2:c.959G>A | NP_055954.1:p.Ser320Asn | |
XM_006710478.1:c.1040G>A | XP_006710541.1:p.Ser347Asn | |
XM_011541070.1:c.1040G>A | XP_011539372.1:p.Ser347Asn | |
XM_006710478.2:c.1040G>A | XP_006710541.1:p.Ser347Asn | |
XM_011541070.2:c.1040G>A | XP_011539372.1:p.Ser347Asn | |
XR_001737057.2:n.1543G>A | ||
XR_001737058.2:n.2328G>A | ||
NM_015139.3:c.959G>A MANE Select | NP_055954.1:p.Ser320Asn |