HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52488099T>A , CM000674.2:g.52488099T>A | GRCh38 |
NC_000012.11:g.52881883T>A , CM000674.1:g.52881883T>A | GRCh37 |
NC_000012.10:g.51168150T>A | NCBI36 |
NG_008298.1:g.10299A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000330722.7:c.1429A>T MANE Select | ENSP00000369317.3:p.Asn477Tyr | |
ENST00000330722.6:c.1429A>T | ENSP00000369317.3:p.Asn477Tyr | |
NM_005554.3:c.1429A>T | NP_005545.1:p.Asn477Tyr | |
NM_005554.4:c.1429A>T MANE Select | NP_005545.1:p.Asn477Tyr |