HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128300907A>C , CM000667.2:g.128300907A>C | GRCh38 |
NC_000005.9:g.127636599A>C , CM000667.1:g.127636599A>C | GRCh37 |
NC_000005.8:g.127664498A>C | NCBI36 |
NG_008750.1:g.242137T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000703783.1:n.2860T>G | ||
ENST00000703785.1:n.2779T>G | ||
ENST00000262464.9:c.6076T>G MANE Select | ENSP00000262464.4:p.Ser2026Ala | |
ENST00000262464.8:c.6076T>G | ENSP00000262464.4:p.Ser2026Ala | |
ENST00000508053.5:c.6076T>G | ENSP00000424571.1:p.Ser2026Ala | |
ENST00000619499.4:c.6073T>G | ENSP00000482132.1:p.Ser2025Ala | |
NM_001999.3:c.6076T>G | NP_001990.2:p.Ser2026Ala | |
XM_017009228.2:c.5923T>G | XP_016864717.1:p.Ser1975Ala | |
NM_001999.4:c.6076T>G MANE Select | NP_001990.2:p.Ser2026Ala |