HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4710625C>T , CM000679.2:g.4710625C>T | GRCh38 |
NC_000017.10:g.4613920C>T , CM000679.1:g.4613920C>T | GRCh37 |
NC_000017.9:g.4560669C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269260.6:c.-97C>T | ENSP00000269260.2:n.-97C>T | |
ENST00000574502.5:c.-97C>T | ENSP00000458371.1:n.-97C>T | |
NM_001257328.1:c.-97C>T | NP_001244257.1:n.-97C>T | |
NM_001257329.1:c.-97C>T | NP_001244258.1:n.-97C>T | |
NM_001257330.1:c.-97C>T | NP_001244259.1:n.-97C>T | |
NM_001257331.1:c.-97C>T | NP_001244260.1:n.-97C>T | |
NM_004313.3:c.-97C>T | NP_004304.1:n.-97C>T | |
NM_199004.1:c.-97C>T | NP_945355.1:n.-97C>T | |
NR_047516.1:n.132C>T | ||
NM_001330064.1:c.-597C>T | NP_001316993.1:n.-597C>T | |
XM_024450752.1:c.-642C>T | XP_024306520.1:n.-642C>T |