HGVS | Genome Assembly |
---|---|
NC_000007.14:g.92518160C>T , CM000669.2:g.92518160C>T | GRCh38 |
NC_000007.13:g.92147474C>T , CM000669.1:g.92147474C>T | GRCh37 |
NC_000007.12:g.91985410C>T | NCBI36 |
NG_008341.1:g.15372G>A | |
NG_008341.2:g.15372G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000248633.9:c.453G>A MANE Select | ENSP00000248633.4:p.Thr151= | |
ENST00000248633.8:c.453G>A | ENSP00000248633.4:p.Thr151= | |
ENST00000428214.5:c.453G>A | ENSP00000394413.1:p.Thr151= | |
ENST00000438045.5:c.273+3942G>A | ENSP00000410438.1:n.273+3942G>A | |
ENST00000484913.5:n.492G>A | ||
NM_000466.2:c.453G>A | NP_000457.1:p.Thr151= | |
NM_001282677.1:c.453G>A | NP_001269606.1:p.Thr151= | |
NM_001282678.1:c.-172G>A | NP_001269607.1:n.-172G>A | |
XR_242246.3:n.549G>A | ||
XR_242246.5:n.500G>A | ||
NM_000466.3:c.453G>A MANE Select | NP_000457.1:p.Thr151= | |
NM_001282677.2:c.453G>A | NP_001269606.1:p.Thr151= | |
NM_001282678.2:c.-172G>A | NP_001269607.1:n.-172G>A |