HGVS | Genome Assembly |
---|---|
NC_000012.12:g.102917270C>A , CM000674.2:g.102917270C>A | GRCh38 |
NC_000012.11:g.103311048C>A , CM000674.1:g.103311048C>A | GRCh37 |
NC_000012.10:g.101835178C>A | NCBI36 |
NG_008690.1:g.5333G>T | |
NG_008690.2:g.46141G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000546708.5:n.493-45G>T | ||
ENST00000546844.1:c.-95-45G>T | ENSP00000446658.1:n.-95-45G>T | |
ENST00000547319.1:n.217-45G>T | ||
ENST00000551337.5:c.-95-45G>T | ENSP00000447620.1:n.-95-45G>T | |
ENST00000553106.5:c.-140G>T | ENSP00000448059.1:n.-140G>T | |
ENST00000635500.1:n.29-4372G>T | ||
NM_000277.1:c.-140G>T | NP_000268.1:n.-140G>T | |
NM_000277.2:c.-140G>T | NP_000268.1:n.-140G>T | |
NM_001354304.1:c.-95-45G>T | NP_001341233.1:n.-95-45G>T | |
NM_001354304.2:c.-95-45G>T | NP_001341233.1:n.-95-45G>T |