HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23423797_23423808dup , CM000676.2:g.23423797_23423808dup | GRCh38 |
NC_000014.8:g.23893006_23893017dup , CM000676.1:g.23893006_23893017dup | GRCh37 |
NC_000014.7:g.22962846_22962857dup | NCBI36 |
NG_007884.1:g.16860_16871dup , LRG_384:g.16860_16871dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.2923-79_2923-68dup MANE Select | ENSP00000347507.3:n.2923-79_2923-68dup | |
ENST00000355349.3:c.2923-79_2923-68dup | ENSP00000347507.3:n.2923-79_2923-68dup | |
NM_000257.3:c.2923-79_2923-68dup | NP_000248.2:n.2923-79_2923-68dup | |
XR_245686.3:n.3029-79_3029-68dup | ||
XM_017021340.1:c.2923-79_2923-68dup | XP_016876829.1:n.2923-79_2923-68dup | |
NM_000257.4:c.2923-79_2923-68dup MANE Select | NP_000248.2:n.2923-79_2923-68dup |