HGVS | Genome Assembly |
---|---|
NC_000015.10:g.66703259A>C , CM000677.2:g.66703259A>C | GRCh38 |
NC_000015.9:g.66995597A>C , CM000677.1:g.66995597A>C | GRCh37 |
NC_000015.8:g.64782651A>C | NCBI36 |
NG_012244.1:g.5924A>C | |
NG_012244.2:g.5924A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000288840.10:c.1A>C MANE Select | ENSP00000288840.5:p.Met1Leu | |
ENST00000288840.9:c.1A>C | ENSP00000288840.5:p.Met1Leu | |
ENST00000557916.5:c.1A>C | ENSP00000452955.1:p.Met1Leu | |
ENST00000612349.1:n.183A>C | ||
NM_005585.4:c.1A>C | NP_005576.3:p.Met1Leu | |
NR_027654.1:n.924A>C | ||
XR_931825.1:n.1160A>C | ||
XR_931826.1:n.1160A>C | ||
XR_931827.1:n.1160A>C | ||
XR_931827.2:n.1150A>C | ||
NM_005585.5:c.1A>C MANE Select | NP_005576.3:p.Met1Leu | |
NR_027654.2:n.1024A>C |