HGVS | Genome Assembly |
---|---|
NC_000008.11:g.63072991T>A , CM000670.2:g.63072991T>A | GRCh38 |
NC_000008.10:g.63985550T>A , CM000670.1:g.63985550T>A | GRCh37 |
NC_000008.9:g.64148104T>A | NCBI36 |
NG_016123.1:g.18063A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260116.5:c.302A>T MANE Select | ENSP00000260116.4:p.His101Leu | |
ENST00000260116.4:c.302A>T | ENSP00000260116.4:p.His101Leu | |
ENST00000521138.1:n.232+12827A>T | ||
NM_000370.3:c.302A>T MANE Select | NP_000361.1:p.His101Leu | |
XM_006716468.2:c.205-8675A>T | XP_006716531.1:n.205-8675A>T | |
XM_006716468.4:c.205-8675A>T | XP_006716531.1:n.205-8675A>T |