Canonical Allele Identifier: CA347189864
Gene: MCEE HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.71351637A>C (hg19) chr2:g.71124507A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124507A>C , CM000664.2:g.71124507A>C GRCh38
NC_000002.11:g.71351637A>C , CM000664.1:g.71351637A>C GRCh37
NC_000002.10:g.71205145A>C NCBI36
NG_008977.1:g.10758T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.77T>G MANE Select ENSP00000244217.5:p.Val26Gly
ENST00000244217.5:c.77T>G ENSP00000244217.5:p.Val26Gly
ENST00000486135.1:c.-209T>G ENSP00000441569.1:n.-209T>G
ENST00000494660.6:c.-209T>G ENSP00000437361.1:n.-209T>G
NM_032601.3:c.77T>G NP_115990.3:p.Val26Gly
XM_005264613.2:c.77T>G XP_005264670.1:p.Val26Gly
XR_939729.1:n.146T>G
XR_939729.2:n.146T>G
NM_032601.4:c.77T>G MANE Select NP_115990.3:p.Val26Gly
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