Canonical Allele Identifier: CA49696468
Gene: MCEE HGNC NCBI

Linked Data

dbSNP Id: rs935512740
MyVariant Identifiers: chr2:g.71124035G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124035G>A , CM000664.2:g.71124035G>A GRCh38
NC_000002.11:g.71351165G>A , CM000664.1:g.71351165G>A GRCh37
NC_000002.10:g.71204673G>A NCBI36
NG_008977.1:g.11230C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.378+171C>T MANE Select ENSP00000244217.5:n.378+171C>T
ENST00000244217.5:c.378+171C>T ENSP00000244217.5:n.378+171C>T
ENST00000413592.5:c.84+333C>T ENSP00000391140.1:n.84+333C>T
NM_032601.3:c.378+171C>T NP_115990.3:n.378+171C>T
XM_005264613.2:c.216+333C>T XP_005264670.1:n.216+333C>T
XR_939729.1:n.447+171C>T
XR_939729.2:n.447+171C>T
NM_032601.4:c.378+171C>T MANE Select NP_115990.3:n.378+171C>T
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