HGVS | Genome Assembly |
---|---|
NC_000014.9:g.76371250G= , CM000676.2:g.76371250G= | GRCh38 |
NC_000014.8:g.76837593G= , CM000676.1:g.76837593G= | GRCh37 |
NC_000014.7:g.75907346G= | NCBI36 |
NG_012278.1:g.4904G= | |
NG_012278.2:g.4904G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000512784.6:c.2+60334G= | ENSP00000424992.2:n.2+60334G= | |
ENST00000505752.5:c.-468G= | ENSP00000423004.1:n.-468G= | |
ENST00000512784.5:c.2+60334G= | ENSP00000424992.1:n.2+60334G= |