HGVS | Genome Assembly |
---|---|
NC_000008.11:g.102238932C>T , CM000670.2:g.102238932C>T | GRCh38 |
NC_000008.10:g.103251160C>T , CM000670.1:g.103251160C>T | GRCh37 |
NC_000008.9:g.103320336C>T | NCBI36 |
NG_016617.1:g.5187G>A , LRG_788:g.5187G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000251810.8:c.-58G>A MANE Select | ENSP00000251810.3:n.-58G>A | |
ENST00000251810.7:c.-58G>A | ENSP00000251810.3:n.-58G>A | |
ENST00000523957.1:c.-58G>A | ENSP00000427830.1:n.-58G>A | |
NM_001172478.1:c.-58G>A | NP_001165949.1:n.-58G>A | |
NM_015713.4:c.-58G>A , LRG_788t2:c.-58G>A | NP_056528.2:n.-58G>A | |
NM_001172478.2:c.-58G>A | NP_001165949.1:n.-58G>A | |
NM_015713.5:c.-58G>A MANE Select | NP_056528.2:n.-58G>A |