HGVS | Genome Assembly |
---|---|
NC_000009.12:g.2729100G= , CM000671.2:g.2729100G= | GRCh38 |
NC_000009.11:g.2729100G= , CM000671.1:g.2729100G= | GRCh37 |
NC_000009.10:g.2719100G= | NCBI36 |
NG_012181.1:g.16575G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382082.4:c.1357-346G= (KCNV2) MANE Select | ENSP00000371514.3:n.1357-346G= | |
ENST00000382082.3:c.1357-346G= (KCNV2) | ENSP00000371514.3:n.1357-346G= | |
ENST00000490444.2:c.277-8568C= (PUM3) | ENSP00000474467.1:n.277-8568C= | |
NM_133497.3:c.1357-346G= (KCNV2) | NP_598004.1:n.1357-346G= | |
XR_929202.1:n.2002-346G= (KCNV2) | ||
XR_929203.1:n.2076G= (KCNV2) | ||
NM_133497.4:c.1357-346G= (KCNV2) MANE Select | NP_598004.1:n.1357-346G= |