HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107701928G>C , CM000669.2:g.107701928G>C | GRCh38 |
NC_000007.13:g.107342373G>C , CM000669.1:g.107342373G>C | GRCh37 |
NC_000007.12:g.107129609G>C | NCBI36 |
NG_008489.1:g.46294G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000644269.2:c.1905G>C MANE Select | ENSP00000494017.1:p.Glu635Asp | |
ENST00000644846.1:c.616G>C | ||
ENST00000265715.7:c.1905G>C | ENSP00000265715.3:p.Glu635Asp | |
ENST00000492030.2:n.192G>C | ||
NM_000441.1:c.1905G>C | NP_000432.1:p.Glu635Asp | |
XM_005250425.1:c.1905G>C | XP_005250482.1:p.Glu635Asp | |
XM_005250425.2:c.1905G>C | XP_005250482.1:p.Glu635Asp | |
XM_017012318.1:c.1827G>C | XP_016867807.1:p.Glu609Asp | |
NM_000441.2:c.1905G>C MANE Select | NP_000432.1:p.Glu635Asp |