HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86575949G>C , CM000670.2:g.86575949G>C | GRCh38 |
NC_000008.10:g.87588177G>C , CM000670.1:g.87588177G>C | GRCh37 |
NC_000008.9:g.87657293G>C | NCBI36 |
NG_016980.1:g.172727C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.2285C>G MANE Select | ENSP00000316605.5:p.Ala762Gly | |
ENST00000681546.1:n.2105C>G | ||
ENST00000681746.1:c.*696C>G | ENSP00000505959.1:n.*696C>G | |
ENST00000320005.5:c.2285C>G | ENSP00000316605.5:p.Ala762Gly | |
ENST00000517327.5:c.276+2740C>G | ENSP00000428329.1:n.276+2740C>G | |
NM_019098.4:c.2285C>G | NP_061971.3:p.Ala762Gly | |
XM_011517138.1:c.1871C>G | XP_011515440.1:p.Ala624Gly | |
XM_011517138.2:c.1871C>G | XP_011515440.1:p.Ala624Gly | |
NM_019098.5:c.2285C>G MANE Select | NP_061971.3:p.Ala762Gly |