HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23431205_23431206insCGTCA , CM000676.2:g.23431205_23431206insCGTCA | GRCh38 |
NC_000014.8:g.23900414_23900415insCGTCA , CM000676.1:g.23900414_23900415insCGTCA | GRCh37 |
NC_000014.7:g.22970254_22970255insCGTCA | NCBI36 |
NG_007884.1:g.9456_9457insTGACG , LRG_384:g.9456_9457insTGACG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.797-207_797-206insTGACG MANE Select | ENSP00000347507.3:n.797-207_797-206insTGACG | |
ENST00000355349.3:c.797-207_797-206insTGACG | ENSP00000347507.3:n.797-207_797-206insTGACG | |
NM_000257.3:c.797-207_797-206insTGACG | NP_000248.2:n.797-207_797-206insTGACG | |
XR_245686.3:n.903-207_903-206insTGACG | ||
XM_017021340.1:c.797-207_797-206insTGACG | XP_016876829.1:n.797-207_797-206insTGACG | |
NM_000257.4:c.797-207_797-206insTGACG MANE Select | NP_000248.2:n.797-207_797-206insTGACG |