Canonical Allele Identifier: CA892637132

Gene: MCEE

Linked Data

• dbSNP Id: rs1392099837
• gnomAD v3: 2-71124063-T-A
• gnomAD v4: 2-71124063-T-A
• MyVariant Identifiers: chr2:g.71351193T>A (hg19) ; chr2:g.71124063T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124063T>A , CM000664.2:g.71124063T>A	GRCh38
NC_000002.11:g.71351193T>A , CM000664.1:g.71351193T>A	GRCh37
NC_000002.10:g.71204701T>A	NCBI36
NG_008977.1:g.11202A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.378+143A>T MANE Select	ENSP00000244217.5:n.378+143A>T
ENST00000244217.5:c.378+143A>T	ENSP00000244217.5:n.378+143A>T
ENST00000413592.5:c.84+305A>T	ENSP00000391140.1:n.84+305A>T
NM_032601.3:c.378+143A>T	NP_115990.3:n.378+143A>T
XM_005264613.2:c.216+305A>T	XP_005264670.1:n.216+305A>T
XR_939729.1:n.447+143A>T
XR_939729.2:n.447+143A>T
NM_032601.4:c.378+143A>T MANE Select	NP_115990.3:n.378+143A>T