HGVS | Genome Assembly |
---|---|
NC_000016.10:g.8797609T>A , CM000678.2:g.8797609T>A | GRCh38 |
NC_000016.9:g.8891466T>A , CM000678.1:g.8891466T>A | GRCh37 |
NC_000016.8:g.8798967T>A | NCBI36 |
NG_009209.1:g.4797T>A | |
NG_033146.1:g.5040A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000333050.7:c.3+3A>T (TMEM186) MANE Select | ENSP00000331640.6:n.3+3A>T | |
ENST00000333050.6:c.3+3A>T (TMEM186) | ENSP00000331640.6:n.3+3A>T | |
ENST00000564869.1:n.31+3A>T (TMEM186) | ||
ENST00000566983.5:c.-15-4190T>A (PMM2) | ENSP00000457956.1:n.-15-4190T>A | |
NM_015421.3:c.3+3A>T (TMEM186) | NP_056236.2:n.3+3A>T | |
NM_015421.4:c.3+3A>T (TMEM186) MANE Select | NP_056236.2:n.3+3A>T |