HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23423449_23423450insTA , CM000676.2:g.23423449_23423450insTA | GRCh38 |
NC_000014.8:g.23892658_23892659insTA , CM000676.1:g.23892658_23892659insTA | GRCh37 |
NC_000014.7:g.22962498_22962499insTA | NCBI36 |
NG_007884.1:g.17213_17214insAT , LRG_384:g.17213_17214insAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3099+98_3099+99insAT MANE Select | ENSP00000347507.3:n.3099+98_3099+99insAT | |
ENST00000355349.3:c.3099+98_3099+99insAT | ENSP00000347507.3:n.3099+98_3099+99insAT | |
NM_000257.3:c.3099+98_3099+99insAT | NP_000248.2:n.3099+98_3099+99insAT | |
XR_245686.3:n.3205+98_3205+99insAT | ||
XM_017021340.1:c.3099+98_3099+99insAT | XP_016876829.1:n.3099+98_3099+99insAT | |
NM_000257.4:c.3099+98_3099+99insAT MANE Select | NP_000248.2:n.3099+98_3099+99insAT |