HGVS | Genome Assembly |
---|---|
NC_000002.12:g.208129642G= , CM000664.2:g.208129642G= | GRCh38 |
NC_000002.11:g.208994366G= , CM000664.1:g.208994366G= | GRCh37 |
NC_000002.10:g.208702611G= | NCBI36 |
NG_008038.1:g.5189C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282141.4:c.51C= MANE Select | ENSP00000282141.3:p.Tyr17= | |
ENST00000282141.3:c.51C= | ENSP00000282141.3:p.Tyr17= | |
NM_020989.3:c.51C= | NP_066269.1:p.Tyr17= | |
NR_038437.1:n.98-7414G= | ||
XM_011510661.1:c.51C= | XP_011508963.1:p.Tyr17= | |
XM_011510662.1:c.51C= | XP_011508964.1:p.Tyr17= | |
XM_011510663.1:c.-79C= | XP_011508965.1:n.-79C= | |
NM_020989.4:c.51C= MANE Select | NP_066269.1:p.Tyr17= |