HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101425589A= , CM000671.2:g.101425589A= | GRCh38 |
NC_000009.11:g.104187871A= , CM000671.1:g.104187871A= | GRCh37 |
NC_000009.10:g.103227692A= | NCBI36 |
NG_012387.1:g.15192T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647789.2:c.663T= MANE Select | ENSP00000497767.1:p.His221= | |
ENST00000648064.1:c.663T= | ENSP00000497990.1:p.His221= | |
ENST00000648758.1:c.663T= | ENSP00000497731.1:p.His221= | |
ENST00000649902.1:c.663T= | ENSP00000497216.1:p.His221= | |
ENST00000374855.8:c.663T= | ENSP00000363988.4:p.His221= | |
ENST00000468981.3:n.190T= | ||
ENST00000616752.1:c.663T= | ENSP00000481363.1:p.His221= | |
NM_000035.3:c.663T= | NP_000026.2:p.His221= | |
NM_000035.4:c.663T= MANE Select | NP_000026.2:p.His221= |