HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119672360T>A , CM000672.2:g.119672360T>A | GRCh38 |
NC_000010.10:g.121431872T>A , CM000672.1:g.121431872T>A | GRCh37 |
NC_000010.9:g.121421862T>A | NCBI36 |
NG_016125.1:g.25991T>A , LRG_742:g.25991T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369085.8:c.613T>A MANE Select | ENSP00000358081.4:p.Tyr205Asn | |
ENST00000369085.7:c.613T>A | ENSP00000358081.3:p.Tyr205Asn | |
ENST00000450186.1:c.439T>A | ENSP00000410036.1:p.Tyr147Asn | |
NM_004281.3:c.613T>A , LRG_742t1:c.613T>A | NP_004272.2:p.Tyr205Asn | |
XM_005270287.1:c.613T>A | XP_005270344.1:p.Tyr205Asn | |
XM_005270287.2:c.613T>A | XP_005270344.1:p.Tyr205Asn | |
NM_004281.4:c.613T>A MANE Select | NP_004272.2:p.Tyr205Asn |