HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213053G>T , CM000667.2:g.1213053G>T | GRCh38 |
NC_000005.9:g.1213168G>T , CM000667.1:g.1213168G>T | GRCh37 |
NC_000005.8:g.1266168G>T | NCBI36 |
NG_008282.1:g.16459G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304460.11:c.664-410G>T MANE Select | ENSP00000305302.10:n.664-410G>T | |
ENST00000304460.10:c.664-410G>T | ENSP00000305302.10:n.664-410G>T | |
ENST00000515652.5:c.572-410G>T | ENSP00000425701.1:n.572-410G>T | |
NM_001003841.2:c.664-410G>T | NP_001003841.1:n.664-410G>T | |
NM_001003841.3:c.664-410G>T MANE Select | NP_001003841.1:n.664-410G>T |