Canonical Allele Identifier: CA49697058

Gene: MCEE

Linked Data

• dbSNP Id: rs373062994
• MyVariant Identifiers: chr2:g.71351714T>A (hg19) ; chr2:g.71124584T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124584T>A , CM000664.2:g.71124584T>A	GRCh38
NC_000002.11:g.71351714T>A , CM000664.1:g.71351714T>A	GRCh37
NC_000002.10:g.71205222T>A	NCBI36
NG_008977.1:g.10681A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.41-41A>T MANE Select	ENSP00000244217.5:n.41-41A>T
ENST00000244217.5:c.41-41A>T	ENSP00000244217.5:n.41-41A>T
ENST00000486135.1:c.-245-41A>T	ENSP00000441569.1:n.-245-41A>T
ENST00000494660.6:c.-245-41A>T	ENSP00000437361.1:n.-245-41A>T
NM_032601.3:c.41-41A>T	NP_115990.3:n.41-41A>T
XM_005264613.2:c.41-41A>T	XP_005264670.1:n.41-41A>T
XR_939729.1:n.110-41A>T
XR_939729.2:n.110-41A>T
NM_032601.4:c.41-41A>T MANE Select	NP_115990.3:n.41-41A>T