HGVS | Genome Assembly |
---|---|
NC_000008.11:g.64624515T= , CM000670.2:g.64624515T= | GRCh38 |
NC_000008.10:g.65537072T= , CM000670.1:g.65537072T= | GRCh37 |
NC_000008.9:g.65699626T= | NCBI36 |
NG_008338.1:g.179277A= | |
NG_008338.2:g.179277A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000310193.4:c.147A= MANE Select | ENSP00000310721.3:p.Ile49= | |
ENST00000310193.3:c.147A= | ENSP00000310721.3:p.Ile49= | |
NM_004820.3:c.147A= | NP_004811.1:p.Ile49= | |
NM_001324112.1:c.147A= | NP_001311041.1:p.Ile49= | |
NM_004820.4:c.147A= | NP_004811.1:p.Ile49= | |
XM_017014002.1:c.213A= | XP_016869491.1:p.Ile71= | |
NM_004820.5:c.147A= MANE Select | NP_004811.1:p.Ile49= | |
NM_001324112.2:c.147A= | NP_001311041.1:p.Ile49= |