HGVS | Genome Assembly |
---|---|
NC_000004.12:g.41746048T>G , CM000666.2:g.41746048T>G | GRCh38 |
NC_000004.11:g.41748065T>G , CM000666.1:g.41748065T>G | GRCh37 |
NC_000004.10:g.41442822T>G | NCBI36 |
NG_008243.1:g.7923A>C , LRG_513:g.7923A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226382.4:c.704A>C MANE Select | ENSP00000226382.2:p.Glu235Ala | |
ENST00000226382.3:c.704A>C | ENSP00000226382.2:p.Glu235Ala | |
ENST00000510424.2:n.525A>C | ||
NM_003924.3:c.704A>C , LRG_513t1:c.704A>C | NP_003915.2:p.Glu235Ala | |
NM_003924.4:c.704A>C MANE Select | NP_003915.2:p.Glu235Ala |