HGVS | Genome Assembly |
---|---|
NC_000009.12:g.6595012A= , CM000671.2:g.6595012A= | GRCh38 |
NC_000009.11:g.6595012A= , CM000671.1:g.6595012A= | GRCh37 |
NC_000009.10:g.6585012A= | NCBI36 |
NG_016397.1:g.55681T= , LRG_643:g.55681T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000321612.8:c.1261+2T= MANE Select | ENSP00000370737.4:n.1261+2T= | |
ENST00000639364.1:n.961+2T= | ||
ENST00000639443.1:n.829+2T= | ||
ENST00000639493.1:n.413+2T= | ||
ENST00000639954.1:n.969+2T= | ||
ENST00000640592.1:n.1144+2T= | ||
ENST00000321612.6:c.1261+2T= | ENSP00000370737.3:n.1261+2T= | |
ENST00000463305.1:n.345+2T= | ||
NM_000170.2:c.1261+2T= , LRG_643t1:c.1261+2T= | NP_000161.2:n.1261+2T= | |
NM_000170.3:c.1261+2T= MANE Select | NP_000161.2:n.1261+2T= |