HGVS | Genome Assembly |
---|---|
NC_000022.11:g.42130885G>A , CM000684.2:g.42130885G>A | GRCh38 |
NC_000022.10:g.42526887G>A , CM000684.1:g.42526887G>A | GRCh37 |
NC_000022.9:g.40856831G>A | NCBI36 |
NG_008376.3:g.4107C>T | |
NG_008376.4:g.4926C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360608.9:c.-94C>T | ENSP00000353820.5:n.-94C>T | |
XM_011529966.1:c.-94C>T | XP_011528268.1:n.-94C>T | |
XM_011529967.1:c.-94C>T | XP_011528269.1:n.-94C>T | |
XM_011529968.1:c.-94C>T | XP_011528270.1:n.-94C>T | |
XM_011529969.1:c.37+412C>T | XP_011528271.1:n.37+412C>T | |
XM_011529970.1:c.-94C>T | XP_011528272.1:n.-94C>T | |
XM_011529971.1:c.37+412C>T | XP_011528273.1:n.37+412C>T | |
XM_011529972.1:c.-94C>T | XP_011528274.1:n.-94C>T | |
XR_430455.2:n.328+197G>A | ||
XR_002958749.1:n.275+197G>A |