HGVS | Genome Assembly |
---|---|
NC_000023.11:g.38370203T>C , CM000685.2:g.38370203T>C | GRCh38 |
NC_000023.10:g.38229456T>C , CM000685.1:g.38229456T>C | GRCh37 |
NC_000023.9:g.38114400T>C | NCBI36 |
NG_008471.1:g.22721T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000039007.5:c.298+326T>C MANE Select | ENSP00000039007.4:n.298+326T>C | |
ENST00000643344.1:c.298+326T>C | ENSP00000496606.1:n.298+326T>C | |
ENST00000039007.4:c.298+326T>C | ENSP00000039007.4:n.298+326T>C | |
ENST00000465127.1:c.172-295918T>C | ENSP00000417050.1:n.172-295918T>C | |
ENST00000488812.1:n.353+363T>C | ||
NM_000531.5:c.298+326T>C | NP_000522.3:n.298+326T>C | |
XM_017029556.1:c.298+326T>C | XP_016885045.1:n.298+326T>C | |
NM_000531.6:c.298+326T>C MANE Select | NP_000522.3:n.298+326T>C |