HGVS | Genome Assembly |
---|---|
NC_000013.11:g.40808421A>G , CM000675.2:g.40808421A>G | GRCh38 |
NC_000013.10:g.41382557A>G , CM000675.1:g.41382557A>G | GRCh37 |
NC_000013.9:g.40280557A>G | NCBI36 |
NG_012248.1:g.24011A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000707033.1:c.623-17A>G (SLC25A15) | ENSP00000516711.1:n.623-17A>G | |
ENST00000338625.9:c.623-17A>G (SLC25A15) MANE Select | ENSP00000342267.4:n.623-17A>G | |
ENST00000338625.8:c.623-17A>G (SLC25A15) | ENSP00000342267.4:n.623-17A>G | |
ENST00000478827.1:n.1110-17A>G (SLC25A15) | ||
NM_014252.3:c.623-17A>G (SLC25A15) | NP_055067.1:n.623-17A>G | |
NR_038258.1:n.623-7697T>C (TPTE2P5) | ||
NR_038259.1:n.452-7697T>C (TPTE2P5) | ||
NM_014252.4:c.623-17A>G (SLC25A15) MANE Select | NP_055067.1:n.623-17A>G |