HGVS | Genome Assembly |
---|---|
NC_000008.11:g.58968506A>G , CM000670.2:g.58968506A>G | GRCh38 |
NC_000008.10:g.59881065A>G , CM000670.1:g.59881065A>G | GRCh37 |
NC_000008.9:g.60043619A>G | NCBI36 |
NG_011993.1:g.155703T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361421.2:c.103-8498T>C MANE Select | ENSP00000354842.1:n.103-8498T>C | |
ENST00000361421.1:c.103-8498T>C | ENSP00000354842.1:n.103-8498T>C | |
NM_014729.2:c.103-8498T>C | NP_055544.1:n.103-8498T>C | |
XM_017014085.1:c.103-28962T>C | XP_016869574.1:n.103-28962T>C | |
NM_014729.3:c.103-8498T>C MANE Select | NP_055544.1:n.103-8498T>C |