HGVS | Genome Assembly |
---|---|
NC_000019.10:g.39248117T>G , CM000681.2:g.39248117T>G | GRCh38 |
NC_000019.9:g.39738757T>G , CM000681.1:g.39738757T>G | GRCh37 |
NC_000019.8:g.44430597T>G | NCBI36 |
NG_042193.1:g.1855A>C | |
NG_055295.1:g.5740A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000606380.2:c.152-122A>C | ENSP00000476098.1:n.152-122A>C | |
ENST00000610963.1:c.151-122A>C | ENSP00000481371.1:n.151-122A>C | |
ENST00000616270.4:c.152-122A>C | ENSP00000480679.1:n.152-122A>C | |
ENST00000634680.1:c.151+312A>C | ENSP00000489240.1:n.151+312A>C | |
ENST00000634967.1:c.152-122A>C | ENSP00000489559.1:n.152-122A>C | |
NR_074079.1:n.429-122A>C |