HGVS | Genome Assembly |
---|---|
NC_000001.11:g.172665577T= , CM000663.2:g.172665577T= | GRCh38 |
NC_000001.10:g.172634717T= , CM000663.1:g.172634717T= | GRCh37 |
NC_000001.9:g.170901340T= | NCBI36 |
NG_007269.1:g.11533T= , LRG_58:g.11533T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000367721.3:c.452-45T= MANE Select | ENSP00000356694.2:n.452-45T= | |
ENST00000340030.4:c.*22-45T= | ENSP00000344739.3:n.*22-45T= | |
ENST00000367721.2:c.452-45T= | ENSP00000356694.2:n.452-45T= | |
NM_000639.2:c.452-45T= | NP_000630.1:n.452-45T= | |
NM_001302746.1:c.*22-45T= | NP_001289675.1:n.*22-45T= | |
NM_000639.3:c.452-45T= MANE Select | NP_000630.1:n.452-45T= | |
NM_001302746.2:c.*22-45T= | NP_001289675.1:n.*22-45T= |