HGVS | Genome Assembly |
---|---|
NC_000008.11:g.63038899A>T , CM000670.2:g.63038899A>T | GRCh38 |
NC_000008.10:g.63951458A>T , CM000670.1:g.63951458A>T | GRCh37 |
NC_000008.9:g.64114012A>T | NCBI36 |
NG_028126.1:g.5153T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000677327.1:n.509T>A | ||
ENST00000679326.1:c.-131T>A | ENSP00000504262.1:n.-131T>A | |
ENST00000260118.6:c.-131T>A | ENSP00000260118.6:n.-131T>A | |
NM_003878.2:c.-131T>A | NP_003869.1:n.-131T>A | |
XM_011517623.1:c.-131T>A | XP_011515925.1:n.-131T>A |