HGVS | Genome Assembly |
---|---|
NC_000001.11:g.172665695G>T , CM000663.2:g.172665695G>T | GRCh38 |
NC_000001.10:g.172634835G>T , CM000663.1:g.172634835G>T | GRCh37 |
NC_000001.9:g.170901458G>T | NCBI36 |
NG_007269.1:g.11651G>T , LRG_58:g.11651G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367721.3:c.525G>T MANE Select | ENSP00000356694.2:p.Lys175Asn | |
ENST00000340030.4:c.*95G>T | ENSP00000344739.3:n.*95G>T | |
ENST00000367721.2:c.525G>T | ENSP00000356694.2:p.Lys175Asn | |
NM_000639.2:c.525G>T | NP_000630.1:p.Lys175Asn | |
NM_001302746.1:c.*95G>T | NP_001289675.1:n.*95G>T | |
NM_000639.3:c.525G>T MANE Select | NP_000630.1:p.Lys175Asn | |
NM_001302746.2:c.*95G>T | NP_001289675.1:n.*95G>T |