HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67583841A>G , CM000673.2:g.67583841A>G | GRCh38 |
NC_000011.9:g.67351312A>G , CM000673.1:g.67351312A>G | GRCh37 |
NC_000011.8:g.67107888A>G | NCBI36 |
NG_012075.1:g.5247A>G , LRG_723:g.5247A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000398603.6:c.-3A>G | ENSP00000381604.1:n.-3A>G | |
ENST00000398606.10:c.-3A>G MANE Select | ENSP00000381607.3:n.-3A>G | |
ENST00000646888.1:c.-3A>G | ENSP00000494477.1:n.-3A>G | |
ENST00000398603.5:c.-3A>G | ENSP00000381604.1:n.-3A>G | |
ENST00000398606.7:c.-3A>G | ENSP00000381607.3:n.-3A>G | |
ENST00000494593.1:n.20A>G | ||
NM_000852.3:c.-3A>G , LRG_723t1:c.-3A>G | NP_000843.1:n.-3A>G | |
NM_000852.4:c.-3A>G MANE Select | NP_000843.1:n.-3A>G |