HGVS | Genome Assembly |
---|---|
NC_000003.12:g.46370346G>T , CM000665.2:g.46370346G>T | GRCh38 |
NC_000003.11:g.46411837G>T , CM000665.1:g.46411837G>T | GRCh37 |
NC_000003.10:g.46386841G>T | NCBI36 |
NG_012637.1:g.5205G>T |
HGVS | Amino-acid change | |
---|---|---|
NM_000579.3:c.-301+148G>T (CCR5) | NP_000570.1:n.-301+148G>T | |
NM_001100168.1:c.-66+148G>T (CCR5) | NP_001093638.1:n.-66+148G>T | |
NR_125406.1:n.565+898C>A (CCR5AS) | ||
NM_000579.4:c.-301+148G>T (CCR5) | NP_000570.1:n.-301+148G>T | |
NM_001100168.2:c.-66+148G>T (CCR5) | NP_001093638.1:n.-66+148G>T |