HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31667429A= , CM000683.2:g.31667429A= | GRCh38 |
NC_000021.8:g.33039742A= , CM000683.1:g.33039742A= | GRCh37 |
NC_000021.7:g.31961613A= | NCBI36 |
NG_008689.1:g.12808A= , LRG_652:g.12808A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.357+54A= MANE Select | ENSP00000270142.7:n.357+54A= | |
ENST00000270142.10:c.357+54A= | ENSP00000270142.6:n.357+54A= | |
ENST00000389995.4:c.300+54A= | ENSP00000374645.4:n.300+54A= | |
ENST00000470944.1:n.1285+54A= | ||
NM_000454.4:c.357+54A= , LRG_652t1:c.357+54A= | NP_000445.1:n.357+54A= | |
NM_000454.5:c.357+54A= MANE Select | NP_000445.1:n.357+54A= |