HGVS | Genome Assembly |
---|---|
NC_000017.11:g.47733453G= , CM000679.2:g.47733453G= | GRCh38 |
NC_000017.10:g.45810819G= , CM000679.1:g.45810819G= | GRCh37 |
NC_000017.9:g.43165818G= | NCBI36 |
NG_012166.1:g.5210G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000177694.2:c.-2G= MANE Select | ENSP00000177694.1:n.-2G= | |
ENST00000177694.1:c.-2G= | ENSP00000177694.1:n.-2G= | |
ENST00000581328.1:n.29G= | ||
NM_013351.1:c.-2G= | NP_037483.1:n.-2G= | |
XM_011524698.1:c.-2G= | XP_011523000.1:n.-2G= | |
NM_013351.2:c.-2G= MANE Select | NP_037483.1:n.-2G= |