HGVS | Genome Assembly |
---|---|
NC_000001.11:g.110064598C= , CM000663.2:g.110064598C= | GRCh38 |
NC_000001.10:g.110607220C= , CM000663.1:g.110607220C= | GRCh37 |
NC_000001.9:g.110408743C= | NCBI36 |
NG_012039.1:g.11103G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647563.2:c.583G= (ALX3) MANE Select | ENSP00000497310.1:p.Ala195= | |
ENST00000649954.1:c.154G= (ALX3) | ENSP00000497035.1:p.Ala52= | |
ENST00000369792.4:c.583G= (ALX3) | ENSP00000358807.3:p.Ala195= | |
ENST00000473429.5:n.4214-7857C= (STRIP1) | ||
NM_006492.2:c.583G= (ALX3) | NP_006483.2:p.Ala195= | |
NM_006492.3:c.583G= (ALX3) MANE Select | NP_006483.2:p.Ala195= |