HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32377506C>T , CM000668.2:g.32377506C>T | GRCh38 |
NC_000006.11:g.32345283C>T , CM000668.1:g.32345283C>T | GRCh37 |
NC_000006.10:g.32453261C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_011515039.1:c.481+11667C>T | XP_011513341.1:n.481+11667C>T | |
XM_011515040.1:c.482-5462C>T | XP_011513342.1:n.482-5462C>T | |
NR_136244.1:n.501-5458C>T | ||
NR_136245.1:n.302+11667C>T |