HGVS | Genome Assembly |
---|---|
NC_000023.11:g.54495275C>G , CM000685.2:g.54495275C>G | GRCh38 |
NC_000023.10:g.54521708C>G , CM000685.1:g.54521708C>G | GRCh37 |
NC_000023.9:g.54538433C>G | NCBI36 |
NG_008054.1:g.5892G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375135.4:c.158G>C MANE Select | ENSP00000364277.3:p.Gly53Ala | |
ENST00000375135.3:c.158G>C | ENSP00000364277.3:p.Gly53Ala | |
NM_004463.2:c.158G>C | NP_004454.2:p.Gly53Ala | |
NM_004463.3:c.158G>C MANE Select | NP_004454.2:p.Gly53Ala |