HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65246001A>T , CM000674.2:g.65246001A>T | GRCh38 |
NC_000012.11:g.65639781A>T , CM000674.1:g.65639781A>T | GRCh37 |
NC_000012.10:g.63926048A>T | NCBI36 |
NG_016210.1:g.81431A>T | |
NG_016210.2:g.81431A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.2572+62A>T MANE Select | ENSP00000308369.2:n.2572+62A>T | |
ENST00000308330.2:c.2572+62A>T | ENSP00000308369.2:n.2572+62A>T | |
ENST00000539442.1:n.554+62A>T | ||
ENST00000544506.1:n.292+62A>T | ||
ENST00000545026.1:n.390+62A>T | ||
NM_001167614.1:c.2569+62A>T | NP_001161086.1:n.2569+62A>T | |
NM_014319.4:c.2572+62A>T | NP_055134.2:n.2572+62A>T | |
NM_014319.5:c.2572+62A>T MANE Select | NP_055134.2:n.2572+62A>T | |
NM_001167614.2:c.2569+62A>T | NP_001161086.1:n.2569+62A>T |