HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52029669G>T , CM000666.2:g.52029669G>T | GRCh38 |
NC_000004.11:g.52895835G>T , CM000666.1:g.52895835G>T | GRCh37 |
NC_000004.10:g.52590592G>T | NCBI36 |
NG_008891.1:g.13651C>A , LRG_204:g.13651C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000381431.10:c.429+9C>A MANE Select | ENSP00000370839.6:n.429+9C>A | |
ENST00000381431.9:c.429+9C>A | ENSP00000370839.5:n.429+9C>A | |
ENST00000506357.5:c.512+9C>A | ||
ENST00000514133.1:c.506+9C>A | ENSP00000425818.1:n.506+9C>A | |
NM_000232.4:c.429+9C>A , LRG_204t1:c.429+9C>A | NP_000223.1:n.429+9C>A | |
XM_006714049.2:c.132+9C>A | XP_006714112.1:n.132+9C>A | |
XM_011534403.1:c.219+9C>A | XP_011532705.1:n.219+9C>A | |
XM_011534404.1:c.132+9C>A | XP_011532706.1:n.132+9C>A | |
NM_000232.5:c.429+9C>A MANE Select | NP_000223.1:n.429+9C>A |