Canonical Allele Identifier: CA426690710

Gene: MCEE

Linked Data

• dbSNP Id: rs1299822001
• gnomAD v2: 2-71351498-C-T
• gnomAD v4: 2-71124368-C-T
• MyVariant Identifiers: chr2:g.71351498C>T (hg19) ; chr2:g.71124368C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124368C>T , CM000664.2:g.71124368C>T	GRCh38
NC_000002.11:g.71351498C>T , CM000664.1:g.71351498C>T	GRCh37
NC_000002.10:g.71205006C>T	NCBI36
NG_008977.1:g.10897G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.216G>A MANE Select	ENSP00000244217.5:p.Gln72=
ENST00000244217.5:c.216G>A	ENSP00000244217.5:p.Gln72=
ENST00000413592.5:c.84G>A	ENSP00000391140.1:p.Gln28=
ENST00000486135.1:c.-70G>A	ENSP00000441569.1:n.-70G>A
ENST00000494660.6:c.-70G>A	ENSP00000437361.1:n.-70G>A
NM_032601.3:c.216G>A	NP_115990.3:p.Gln72=
XM_005264613.2:c.216G>A	XP_005264670.1:p.Gln72=
XR_939729.1:n.285G>A
XR_939729.2:n.285G>A
NM_032601.4:c.216G>A MANE Select	NP_115990.3:p.Gln72=