HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41612459C>T , CM000679.2:g.41612459C>T | GRCh38 |
NC_000017.10:g.39768711C>T , CM000679.1:g.39768711C>T | GRCh37 |
NC_000017.9:g.37022237C>T | NCBI36 |
NG_008301.1:g.5369G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301653.9:c.230G>A MANE Select | ENSP00000301653.3:p.Ser77Asn | |
ENST00000301653.8:c.230G>A | ENSP00000301653.3:p.Ser77Asn | |
ENST00000588319.1:n.307G>A | ||
ENST00000593067.1:c.-312-173G>A | ENSP00000467124.1:n.-312-173G>A | |
NM_005557.3:c.230G>A | NP_005548.2:p.Ser77Asn | |
NM_005557.4:c.230G>A MANE Select | NP_005548.2:p.Ser77Asn |