HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23393599C>G , CM000676.2:g.23393599C>G | GRCh38 |
NC_000014.8:g.23862808C>G , CM000676.1:g.23862808C>G | GRCh37 |
NC_000014.7:g.22932648C>G | NCBI36 |
NG_023444.1:g.19679G>C , LRG_389:g.19679G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000405093.9:c.2928+67G>C MANE Select | ENSP00000386041.3:n.2928+67G>C | |
ENST00000356287.3:c.2928+67G>C | ENSP00000348634.3:n.2928+67G>C | |
ENST00000405093.7:c.2928+67G>C | ENSP00000386041.3:n.2928+67G>C | |
NM_002471.3:c.2928+67G>C , LRG_389t1:c.2928+67G>C | NP_002462.2:n.2928+67G>C | |
NM_002471.4:c.2928+67G>C MANE Select | NP_002462.2:n.2928+67G>C |