HGVS | Genome Assembly |
---|---|
NC_000009.12:g.129818773A>T , CM000671.2:g.129818773A>T | GRCh38 |
NC_000009.11:g.132581052A>T , CM000671.1:g.132581052A>T | GRCh37 |
NC_000009.10:g.131620873A>T | NCBI36 |
NG_008049.1:g.10390T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000351698.5:c.592T>A MANE Select | ENSP00000345719.4:p.Tyr198Asn | |
ENST00000651202.1:c.688T>A | ENSP00000498222.1:p.Tyr230Asn | |
ENST00000351698.4:c.592T>A | ENSP00000345719.4:p.Tyr198Asn | |
ENST00000473604.2:n.702T>A | ||
ENST00000474192.1:n.9T>A | ||
NM_000113.2:c.592T>A | NP_000104.1:p.Tyr198Asn | |
XR_929731.1:n.752T>A | ||
XR_929731.3:n.620T>A | ||
NM_000113.3:c.592T>A MANE Select | NP_000104.1:p.Tyr198Asn |