HGVS | Genome Assembly |
---|---|
NC_000001.11:g.147908161C>A , CM000663.2:g.147908161C>A | GRCh38 |
NC_000001.10:g.147380288C>A , CM000663.1:g.147380288C>A | GRCh37 |
NC_000001.9:g.145846912C>A | NCBI36 |
NG_016242.1:g.10343C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369235.2:c.206C>A MANE Select | ENSP00000358238.1:p.Ala69Asp | |
ENST00000369235.1:c.206C>A | ENSP00000358238.1:p.Ala69Asp | |
NM_005267.4:c.206C>A | NP_005258.2:p.Ala69Asp | |
XM_011509416.1:c.206C>A | XP_011507718.1:p.Ala69Asp | |
XM_011509417.1:c.206C>A | XP_011507719.1:p.Ala69Asp | |
XM_011509417.2:c.206C>A | XP_011507719.1:p.Ala69Asp | |
XR_002956281.1:n.1121C>A | ||
NM_005267.5:c.206C>A MANE Select | NP_005258.2:p.Ala69Asp |