HGVS | Genome Assembly |
---|---|
NC_000012.12:g.69350142C>A , CM000674.2:g.69350142C>A | GRCh38 |
NC_000012.11:g.69743922C>A , CM000674.1:g.69743922C>A | GRCh37 |
NC_000012.10:g.68030189C>A | NCBI36 |
NG_008195.1:g.6789C>A , LRG_768:g.6789C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261267.7:c.171C>A MANE Select | ENSP00000261267.2:p.Asn57Lys | |
ENST00000261267.6:c.171C>A | ENSP00000261267.2:p.Asn57Lys | |
ENST00000548839.1:c.171C>A | ENSP00000449969.1:p.Asn57Lys | |
ENST00000549690.1:c.171C>A | ENSP00000449898.1:p.Asn57Lys | |
NM_000239.2:c.171C>A , LRG_768t1:c.171C>A | NP_000230.1:p.Asn57Lys | |
NM_000239.3:c.171C>A MANE Select | NP_000230.1:p.Asn57Lys |