HGVS | Genome Assembly |
---|---|
NC_000020.11:g.31819978A= , CM000682.2:g.31819978A= | GRCh38 |
NC_000020.10:g.30407781A= , CM000682.1:g.30407781A= | GRCh37 |
NC_000020.9:g.29871442A= | NCBI36 |
NG_012847.1:g.5604A= , LRG_392:g.5604A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375985.5:c.53-148A= MANE Select | ENSP00000365152.4:n.53-148A= | |
ENST00000375985.4:c.53-148A= | ENSP00000365152.4:n.53-148A= | |
ENST00000375994.6:c.53-148A= | ENSP00000365162.2:n.53-148A= | |
NM_033118.3:c.53-148A= , LRG_392t1:c.53-148A= | NP_149109.1:n.53-148A= | |
XR_244155.1:n.218-148A= | ||
NM_033118.4:c.53-148A= MANE Select | NP_149109.1:n.53-148A= |