HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52451634T>A , CM000674.2:g.52451634T>A | GRCh38 |
NC_000012.11:g.52845418T>A , CM000674.1:g.52845418T>A | GRCh37 |
NC_000012.10:g.51131685T>A | NCBI36 |
NG_008299.1:g.5493A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252252.4:c.445A>T MANE Select | ENSP00000252252.3:p.Asn149Tyr | |
ENST00000252252.3:c.445A>T | ENSP00000252252.3:p.Asn149Tyr | |
NM_005555.3:c.445A>T | NP_005546.2:p.Asn149Tyr | |
NM_005555.4:c.445A>T MANE Select | NP_005546.2:p.Asn149Tyr |