Canonical Allele Identifier: CA1259891125
Gene: MCEE HGNC NCBI

Linked Data

dbSNP Id: rs1241903696

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71123961G>T , CM000664.2:g.71123961G>T GRCh38
NC_000002.11:g.71351091G>T , CM000664.1:g.71351091G>T GRCh37
NC_000002.10:g.71204599G>T NCBI36
NG_008977.1:g.11304C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.378+245C>A MANE Select ENSP00000244217.5:n.378+245C>A
ENST00000244217.5:c.378+245C>A ENSP00000244217.5:n.378+245C>A
ENST00000413592.5:c.84+407C>A ENSP00000391140.1:n.84+407C>A
NM_032601.3:c.378+245C>A NP_115990.3:n.378+245C>A
XM_005264613.2:c.216+407C>A XP_005264670.1:n.216+407C>A
XR_939729.1:n.447+245C>A
XR_939729.2:n.447+245C>A
NM_032601.4:c.378+245C>A MANE Select NP_115990.3:n.378+245C>A