HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52451633T>G , CM000674.2:g.52451633T>G | GRCh38 |
NC_000012.11:g.52845417T>G , CM000674.1:g.52845417T>G | GRCh37 |
NC_000012.10:g.51131684T>G | NCBI36 |
NG_008299.1:g.5494A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252252.4:c.446A>C MANE Select | ENSP00000252252.3:p.Asn149Thr | |
ENST00000252252.3:c.446A>C | ENSP00000252252.3:p.Asn149Thr | |
NM_005555.3:c.446A>C | NP_005546.2:p.Asn149Thr | |
NM_005555.4:c.446A>C MANE Select | NP_005546.2:p.Asn149Thr |