HGVS | Genome Assembly |
---|---|
NC_000019.10:g.12887122C= , CM000681.2:g.12887122C= | GRCh38 |
NC_000019.9:g.12997936C= , CM000681.1:g.12997936C= | GRCh37 |
NC_000019.8:g.12858936C= | NCBI36 |
NG_009292.1:g.963C= | |
NG_013087.1:g.5082G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264834.6:c.19G= MANE Select | ENSP00000264834.3:p.Ala7= | |
ENST00000264834.4:c.19G= | ENSP00000264834.3:p.Ala7= | |
NM_006563.3:c.19G= | NP_006554.1:p.Ala7= | |
XM_011527642.1:c.-185G= | XP_011525944.1:n.-185G= | |
NM_006563.4:c.19G= | NP_006554.1:p.Ala7= | |
XM_011527642.2:c.-185G= | XP_011525944.1:n.-185G= | |
NM_006563.5:c.19G= MANE Select | NP_006554.1:p.Ala7= |