HGVS | Genome Assembly |
---|---|
NC_000005.10:g.37249428C>A , CM000667.2:g.37249428C>A | GRCh38 |
NC_000005.9:g.37249530C>A , CM000667.1:g.37249530C>A | GRCh37 |
NC_000005.8:g.37285287C>A | NCBI36 |
NG_032772.1:g.5001G>T | |
NG_032772.2:g.5001G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000425232.6:c.-231G>T (CPLANE1) | ENSP00000389014.2:n.-231G>T | |
NM_023073.3:c.-231G>T (CPLANE1) | NP_075561.3:n.-231G>T | |
XR_925921.1:n.171+207C>A (CPLANE1-AS1) | ||
NR_134263.1:n.176+207C>A (CPLANE1-AS1) | ||
XM_005248345.4:c.-231G>T (CPLANE1) | XP_005248402.1:n.-231G>T | |
XM_005248346.4:c.-231G>T (CPLANE1) | XP_005248403.1:n.-231G>T | |
XM_005248347.4:c.-231G>T (CPLANE1) | XP_005248404.1:n.-231G>T | |
XM_005248349.4:c.-231G>T (CPLANE1) | XP_005248406.1:n.-231G>T | |
XM_005248350.4:c.-231G>T (CPLANE1) | XP_005248407.1:n.-231G>T |