HGVS | Genome Assembly |
---|---|
NC_000016.10:g.8797619C>A , CM000678.2:g.8797619C>A | GRCh38 |
NC_000016.9:g.8891476C>A , CM000678.1:g.8891476C>A | GRCh37 |
NC_000016.8:g.8798977C>A | NCBI36 |
NG_009209.1:g.4807C>A | |
NG_033146.1:g.5030G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000333050.7:c.-5G>T (TMEM186) MANE Select | ENSP00000331640.6:n.-5G>T | |
ENST00000333050.6:c.-5G>T (TMEM186) | ENSP00000331640.6:n.-5G>T | |
ENST00000564869.1:n.24G>T (TMEM186) | ||
ENST00000566983.5:c.-15-4180C>A (PMM2) | ENSP00000457956.1:n.-15-4180C>A | |
NM_015421.3:c.-5G>T (TMEM186) | NP_056236.2:n.-5G>T | |
NM_015421.4:c.-5G>T (TMEM186) MANE Select | NP_056236.2:n.-5G>T |