HGVS | Genome Assembly |
---|---|
NC_000009.12:g.2729331A= , CM000671.2:g.2729331A= | GRCh38 |
NC_000009.11:g.2729331A= , CM000671.1:g.2729331A= | GRCh37 |
NC_000009.10:g.2719331A= | NCBI36 |
NG_012181.1:g.16806A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382082.4:c.1357-115A= (KCNV2) MANE Select | ENSP00000371514.3:n.1357-115A= | |
ENST00000382082.3:c.1357-115A= (KCNV2) | ENSP00000371514.3:n.1357-115A= | |
ENST00000490444.2:c.277-8799T= (PUM3) | ENSP00000474467.1:n.277-8799T= | |
NM_133497.3:c.1357-115A= (KCNV2) | NP_598004.1:n.1357-115A= | |
XR_929202.1:n.2002-115A= (KCNV2) | ||
XR_929203.1:n.2307A= (KCNV2) | ||
NM_133497.4:c.1357-115A= (KCNV2) MANE Select | NP_598004.1:n.1357-115A= |