HGVS | Genome Assembly |
---|---|
NC_000023.11:g.134498337G= , CM000685.2:g.134498337G= | GRCh38 |
NC_000023.10:g.133632367G= , CM000685.1:g.133632367G= | GRCh37 |
NC_000023.9:g.133460033G= | NCBI36 |
NG_012329.1:g.43193G= | |
NG_012329.2:g.43193G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000298556.8:c.486-53G= MANE Select | ENSP00000298556.7:n.486-53G= | |
ENST00000298556.7:c.486-53G= | ENSP00000298556.7:n.486-53G= | |
ENST00000462974.5:n.644-53G= | ||
ENST00000475720.1:n.444-53G= | ||
NM_000194.2:c.486-53G= | NP_000185.1:n.486-53G= | |
XM_011531328.1:c.504-53G= | XP_011529630.1:n.504-53G= | |
NM_000194.3:c.486-53G= MANE Select | NP_000185.1:n.486-53G= |