HGVS | Genome Assembly |
---|---|
NC_000019.10:g.39248157T>G , CM000681.2:g.39248157T>G | GRCh38 |
NC_000019.9:g.39738797T>G , CM000681.1:g.39738797T>G | GRCh37 |
NC_000019.8:g.44430637T>G | NCBI36 |
NG_042193.1:g.1815A>C | |
NG_055295.1:g.5700A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000606380.2:c.152-162A>C | ENSP00000476098.1:n.152-162A>C | |
ENST00000610963.1:c.151-162A>C | ENSP00000481371.1:n.151-162A>C | |
ENST00000616270.4:c.152-162A>C | ENSP00000480679.1:n.152-162A>C | |
ENST00000634680.1:c.151+272A>C | ENSP00000489240.1:n.151+272A>C | |
ENST00000634967.1:c.152-162A>C | ENSP00000489559.1:n.152-162A>C | |
NR_074079.1:n.429-162A>C |