Canonical Allele Identifier: CA426691930
Gene: MCEE HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.71351624G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124494G>C , CM000664.2:g.71124494G>C GRCh38
NC_000002.11:g.71351624G>C , CM000664.1:g.71351624G>C GRCh37
NC_000002.10:g.71205132G>C NCBI36
NG_008977.1:g.10771C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.90C>G MANE Select ENSP00000244217.5:p.Ser30=
ENST00000244217.5:c.90C>G ENSP00000244217.5:p.Ser30=
ENST00000486135.1:c.-196C>G ENSP00000441569.1:n.-196C>G
ENST00000494660.6:c.-196C>G ENSP00000437361.1:n.-196C>G
NM_032601.3:c.90C>G NP_115990.3:p.Ser30=
XM_005264613.2:c.90C>G XP_005264670.1:p.Ser30=
XR_939729.1:n.159C>G
XR_939729.2:n.159C>G
NM_032601.4:c.90C>G MANE Select NP_115990.3:p.Ser30=
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