HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43776177C>T , CM000683.2:g.43776177C>T | GRCh38 |
NC_000021.8:g.45196058C>T , CM000683.1:g.45196058C>T | GRCh37 |
NC_000021.7:g.44020486C>T | NCBI36 |
NG_011545.1:g.5202G>A , LRG_485:g.5202G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291568.7:c.66+27G>A MANE Select | ENSP00000291568.6:n.66+27G>A | |
ENST00000480147.3:n.92G>A | ||
ENST00000639959.1:c.35+27G>A | ||
ENST00000640406.1:c.66+27G>A | ENSP00000492672.1:n.66+27G>A | |
ENST00000675996.1:n.154G>A | ||
ENST00000291568.5:c.66+27G>A | ENSP00000291568.5:n.66+27G>A | |
ENST00000480147.1:n.103+27G>A | ||
NM_000100.3:c.66+27G>A , LRG_485t1:c.66+27G>A | NP_000091.1:n.66+27G>A | |
NM_000100.4:c.66+27G>A MANE Select | NP_000091.1:n.66+27G>A |