Canonical Allele Identifier: CA1259891372
Gene: MCEE HGNC NCBI

Linked Data

dbSNP Id: rs1673179323
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124561C>T , CM000664.2:g.71124561C>T GRCh38
NC_000002.11:g.71351691C>T , CM000664.1:g.71351691C>T GRCh37
NC_000002.10:g.71205199C>T NCBI36
NG_008977.1:g.10704G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.41-18G>A MANE Select ENSP00000244217.5:n.41-18G>A
ENST00000244217.5:c.41-18G>A ENSP00000244217.5:n.41-18G>A
ENST00000486135.1:c.-245-18G>A ENSP00000441569.1:n.-245-18G>A
ENST00000494660.6:c.-245-18G>A ENSP00000437361.1:n.-245-18G>A
NM_032601.3:c.41-18G>A NP_115990.3:n.41-18G>A
XM_005264613.2:c.41-18G>A XP_005264670.1:n.41-18G>A
XR_939729.1:n.110-18G>A
XR_939729.2:n.110-18G>A
NM_032601.4:c.41-18G>A MANE Select NP_115990.3:n.41-18G>A
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