HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149927777C= , CM000663.2:g.149927777C= | GRCh38 |
NC_000001.10:g.149899669C= , CM000663.1:g.149899669C= | GRCh37 |
NC_000001.9:g.148166293C= | NCBI36 |
NG_032777.1:g.5476G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.9:c.-18G= MANE Select | ENSP00000271628.8:n.-18G= | |
ENST00000271628.8:c.-18G= | ENSP00000271628.8:n.-18G= | |
NM_005850.4:c.-18G= | NP_005841.1:n.-18G= | |
NM_005850.5:c.-18G= MANE Select | NP_005841.1:n.-18G= |