HGVS | Genome Assembly |
---|---|
NC_000008.11:g.63038961C>A , CM000670.2:g.63038961C>A | GRCh38 |
NC_000008.10:g.63951520C>A , CM000670.1:g.63951520C>A | GRCh37 |
NC_000008.9:g.64114074C>A | NCBI36 |
NG_028126.1:g.5091G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000677327.1:n.447G>T | ||
ENST00000679326.1:c.-193G>T | ENSP00000504262.1:n.-193G>T | |
ENST00000260118.6:c.-193G>T | ENSP00000260118.6:n.-193G>T | |
NM_003878.2:c.-193G>T | NP_003869.1:n.-193G>T | |
XM_011517623.1:c.-193G>T | XP_011515925.1:n.-193G>T |