HGVS | Genome Assembly |
---|---|
NC_000006.12:g.38696981C>T , CM000668.2:g.38696981C>T | GRCh38 |
NC_000006.11:g.38664757C>T , CM000668.1:g.38664757C>T | GRCh37 |
NC_000006.10:g.38772735C>T | NCBI36 |
NG_012074.1:g.11196G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373365.5:c.84+5990G>A MANE Select | ENSP00000362463.3:n.84+5990G>A | |
ENST00000373365.4:c.84+5990G>A | ENSP00000362463.3:n.84+5990G>A | |
NM_006708.2:c.84+5990G>A | NP_006699.2:n.84+5990G>A | |
NM_006708.3:c.84+5990G>A MANE Select | NP_006699.2:n.84+5990G>A |