HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23422473T>A , CM000676.2:g.23422473T>A | GRCh38 |
NC_000014.8:g.23891682T>A , CM000676.1:g.23891682T>A | GRCh37 |
NC_000014.7:g.22961522T>A | NCBI36 |
NG_007884.1:g.18189A>T , LRG_384:g.18189A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3100-148A>T MANE Select | ENSP00000347507.3:n.3100-148A>T | |
ENST00000355349.3:c.3100-148A>T | ENSP00000347507.3:n.3100-148A>T | |
NM_000257.3:c.3100-148A>T | NP_000248.2:n.3100-148A>T | |
XR_245686.3:n.3206-148A>T | ||
XM_017021340.1:c.3100-148A>T | XP_016876829.1:n.3100-148A>T | |
NM_000257.4:c.3100-148A>T MANE Select | NP_000248.2:n.3100-148A>T |