HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23421236_23421253dup , CM000676.2:g.23421236_23421253dup | GRCh38 |
NC_000014.8:g.23890445_23890462dup , CM000676.1:g.23890445_23890462dup | GRCh37 |
NC_000014.7:g.22960285_22960302dup | NCBI36 |
NG_007884.1:g.19410_19427dup , LRG_384:g.19410_19427dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3246-204_3246-187dup MANE Select | ENSP00000347507.3:n.3246-204_3246-187dup | |
ENST00000355349.3:c.3246-204_3246-187dup | ENSP00000347507.3:n.3246-204_3246-187dup | |
NM_000257.3:c.3246-204_3246-187dup | NP_000248.2:n.3246-204_3246-187dup | |
XR_245686.3:n.3354-204_3354-187dup | ||
XM_017021340.1:c.3246-204_3246-187dup | XP_016876829.1:n.3246-204_3246-187dup | |
NM_000257.4:c.3246-204_3246-187dup MANE Select | NP_000248.2:n.3246-204_3246-187dup |