Canonical Allele Identifier: CA1259891145
Gene: MCEE HGNC NCBI

Linked Data

dbSNP Id: rs1673157546
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124033A>T , CM000664.2:g.71124033A>T GRCh38
NC_000002.11:g.71351163A>T , CM000664.1:g.71351163A>T GRCh37
NC_000002.10:g.71204671A>T NCBI36
NG_008977.1:g.11232T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.378+173T>A MANE Select ENSP00000244217.5:n.378+173T>A
ENST00000244217.5:c.378+173T>A ENSP00000244217.5:n.378+173T>A
ENST00000413592.5:c.84+335T>A ENSP00000391140.1:n.84+335T>A
NM_032601.3:c.378+173T>A NP_115990.3:n.378+173T>A
XM_005264613.2:c.216+335T>A XP_005264670.1:n.216+335T>A
XR_939729.1:n.447+173T>A
XR_939729.2:n.447+173T>A
NM_032601.4:c.378+173T>A MANE Select NP_115990.3:n.378+173T>A
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Search 100 bp 3'