HGVS | Genome Assembly |
---|---|
NC_000012.12:g.19626761A>T , CM000674.2:g.19626761A>T | GRCh38 |
NC_000012.11:g.19779695A>T , CM000674.1:g.19779695A>T | GRCh37 |
NC_000012.10:g.19670962A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000512223.6:c.339-93872A>T | ENSP00000445587.1:n.339-93872A>T | |
XR_242921.2:n.252+23448A>T | ||
XR_931408.1:n.76+755A>T | ||
XR_001749034.2:n.472-23635A>T | ||
XR_001749035.1:n.525+23448A>T | ||
XR_001749036.1:n.526-22937A>T | ||
XR_001749037.1:n.275+23448A>T | ||
XR_002957408.1:n.133+755A>T |