HGVS | Genome Assembly |
---|---|
NC_000001.11:g.110064566C>G , CM000663.2:g.110064566C>G | GRCh38 |
NC_000001.10:g.110607188C>G , CM000663.1:g.110607188C>G | GRCh37 |
NC_000001.9:g.110408711C>G | NCBI36 |
NG_012039.1:g.11135G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647563.2:c.594+21G>C (ALX3) MANE Select | ENSP00000497310.1:n.594+21G>C | |
ENST00000649954.1:c.165+21G>C (ALX3) | ENSP00000497035.1:n.165+21G>C | |
ENST00000369792.4:c.594+21G>C (ALX3) | ENSP00000358807.3:n.594+21G>C | |
ENST00000473429.5:n.4214-7889C>G (STRIP1) | ||
NM_006492.2:c.594+21G>C (ALX3) | NP_006483.2:n.594+21G>C | |
NM_006492.3:c.594+21G>C (ALX3) MANE Select | NP_006483.2:n.594+21G>C |