HGVS | Genome Assembly |
---|---|
NC_000008.11:g.17604047C>T , CM000670.2:g.17604047C>T | GRCh38 |
NC_000008.10:g.17461556C>T , CM000670.1:g.17461556C>T | GRCh37 |
NC_000008.9:g.17505833C>T | NCBI36 |
NG_023332.1:g.32615C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251630.11:c.353+14282C>T MANE Select | ENSP00000251630.4:n.353+14282C>T | |
ENST00000673645.1:c.353+14282C>T | ENSP00000501219.1:n.353+14282C>T | |
ENST00000251630.10:c.353+14282C>T | ENSP00000251630.4:n.353+14282C>T | |
ENST00000541323.1:c.353+14282C>T | ENSP00000444211.1:n.353+14282C>T | |
NM_006207.2:c.353+14282C>T | NP_006198.1:n.353+14282C>T | |
XM_011544558.1:c.353+14282C>T | XP_011542860.1:n.353+14282C>T | |
NM_001372073.1:c.353+14282C>T MANE Select | NP_001359002.1:n.353+14282C>T |