HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128305056T= , CM000667.2:g.128305056T= | GRCh38 |
NC_000005.9:g.127640748T= , CM000667.1:g.127640748T= | GRCh37 |
NC_000005.8:g.127668647T= | NCBI36 |
NG_008750.1:g.237988A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000703783.1:n.2485A= | ||
ENST00000703785.1:n.2404A= | ||
ENST00000262464.9:c.5701A= MANE Select | ENSP00000262464.4:p.Asn1901= | |
ENST00000262464.8:c.5701A= | ENSP00000262464.4:p.Asn1901= | |
ENST00000508053.5:c.5701A= | ENSP00000424571.1:p.Asn1901= | |
ENST00000619499.4:c.5698A= | ENSP00000482132.1:p.Asn1900= | |
NM_001999.3:c.5701A= | NP_001990.2:p.Asn1901= | |
XM_017009228.2:c.5548A= | XP_016864717.1:p.Asn1850= | |
NM_001999.4:c.5701A= MANE Select | NP_001990.2:p.Asn1901= |