HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31200059A>C , CM000668.2:g.31200059A>C | GRCh38 |
NC_000006.11:g.31167836A>C , CM000668.1:g.31167836A>C | GRCh37 |
NC_000006.10:g.31275815A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000383331.4:c.123+2177A>C | ||
ENST00000414008.2:n.166A>C | ||
ENST00000424675.1:c.44+1878A>C | ||
NR_026791.1:n.123+2177A>C |