HGVS | Genome Assembly |
---|---|
NC_000007.14:g.32404836A>C , CM000669.2:g.32404836A>C | GRCh38 |
NC_000007.13:g.32444448A>C , CM000669.1:g.32444448A>C | GRCh37 |
NC_000007.12:g.32410973A>C | NCBI36 |
NG_051183.1:g.28389T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000672256.1:c.310+22986T>G | ENSP00000499831.1:n.310+22986T>G | |
NM_001322059.1:c.310+22986T>G | NP_001308988.1:n.310+22986T>G | |
NM_001322059.2:c.310+22986T>G | NP_001308988.1:n.310+22986T>G |