HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47332116T>G , CM000673.2:g.47332116T>G | GRCh38 |
NC_000011.9:g.47353667T>G , CM000673.1:g.47353667T>G | GRCh37 |
NC_000011.8:g.47310243T>G | NCBI36 |
NG_007667.1:g.25587A>C , LRG_386:g.25587A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000545968.6:c.3770A>C MANE Select | ENSP00000442795.1:p.Asn1257Thr | |
ENST00000256993.8:c.3770A>C | ENSP00000256993.5:p.Asn1257Thr | |
ENST00000399249.6:c.3770A>C | ENSP00000382193.2:p.Asn1257Thr | |
ENST00000545968.5:c.3770A>C | ENSP00000442795.1:p.Asn1257Thr | |
NM_000256.3:c.3770A>C , LRG_386t1:c.3770A>C MANE Select | NP_000247.2:p.Asn1257Thr | |
XM_011520117.1:c.3752A>C | XP_011518419.1:p.Asn1251Thr | |
XM_011520118.1:c.3689A>C | XP_011518420.1:p.Asn1230Thr |