Canonical Allele Identifier: CA426692045
Gene: MCEE HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.71351657A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124527A>C , CM000664.2:g.71124527A>C GRCh38
NC_000002.11:g.71351657A>C , CM000664.1:g.71351657A>C GRCh37
NC_000002.10:g.71205165A>C NCBI36
NG_008977.1:g.10738T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.57T>G MANE Select ENSP00000244217.5:p.Leu19=
ENST00000244217.5:c.57T>G ENSP00000244217.5:p.Leu19=
ENST00000486135.1:c.-229T>G ENSP00000441569.1:n.-229T>G
ENST00000494660.6:c.-229T>G ENSP00000437361.1:n.-229T>G
NM_032601.3:c.57T>G NP_115990.3:p.Leu19=
XM_005264613.2:c.57T>G XP_005264670.1:p.Leu19=
XR_939729.1:n.126T>G
XR_939729.2:n.126T>G
NM_032601.4:c.57T>G MANE Select NP_115990.3:p.Leu19=
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