HGVS | Genome Assembly |
---|---|
NC_000009.12:g.2729804G>A , CM000671.2:g.2729804G>A | GRCh38 |
NC_000009.11:g.2729804G>A , CM000671.1:g.2729804G>A | GRCh37 |
NC_000009.10:g.2719804G>A | NCBI36 |
NG_012181.1:g.17279G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382082.4:c.*77G>A (KCNV2) MANE Select | ENSP00000371514.3:n.*77G>A | |
ENST00000382082.3:c.*77G>A (KCNV2) | ENSP00000371514.3:n.*77G>A | |
ENST00000490444.2:c.277-9272C>T (PUM3) | ENSP00000474467.1:n.277-9272C>T | |
NM_133497.3:c.*77G>A (KCNV2) | NP_598004.1:n.*77G>A | |
NM_133497.4:c.*77G>A (KCNV2) MANE Select | NP_598004.1:n.*77G>A |