HGVS | Genome Assembly |
---|---|
NC_000002.12:g.203867825C>A , CM000664.2:g.203867825C>A | GRCh38 |
NC_000002.11:g.204732548C>A , CM000664.1:g.204732548C>A | GRCh37 |
NC_000002.10:g.204440793C>A | NCBI36 |
NG_011502.1:g.5040C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696049.1:c.-118C>A | ENSP00000512353.1:n.-118C>A | |
ENST00000696479.1:c.48-93C>A | ENSP00000512655.1:n.48-93C>A | |
ENST00000648405.2:c.-118C>A MANE Select | ENSP00000497102.1:n.-118C>A | |
ENST00000302823.7:c.-118C>A | ENSP00000303939.3:n.-118C>A | |
NM_001037631.2:c.-118C>A | NP_001032720.1:n.-118C>A | |
NM_005214.4:c.-118C>A | NP_005205.2:n.-118C>A | |
XR_241294.1:n.23C>A | ||
NM_001037631.3:c.-118C>A | NP_001032720.1:n.-118C>A | |
NM_005214.5:c.-118C>A MANE Select | NP_005205.2:n.-118C>A |