HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57763703G>T , CM000674.2:g.57763703G>T | GRCh38 |
NC_000012.11:g.58157486G>T , CM000674.1:g.58157486G>T | GRCh37 |
NC_000012.10:g.56443753G>T | NCBI36 |
NG_007076.1:g.8491C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000713544.1:c.1402C>A | ENSP00000518840.1:p.His468Asn | |
ENST00000713545.1:c.*326C>A | ENSP00000518841.1:n.*326C>A | |
ENST00000228606.9:c.1321C>A MANE Select | ENSP00000228606.4:p.His441Asn | |
ENST00000228606.8:c.1321C>A | ENSP00000228606.4:p.His441Asn | |
ENST00000547344.5:n.1460C>A | ||
NM_000785.3:c.1321C>A | NP_000776.1:p.His441Asn | |
NM_000785.4:c.1321C>A MANE Select | NP_000776.1:p.His441Asn |