Canonical Allele Identifier: CA426690765

Gene: MCEE

Linked Data

• MyVariant Identifiers: chr2:g.71351504C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71124374C>G , CM000664.2:g.71124374C>G	GRCh38
NC_000002.11:g.71351504C>G , CM000664.1:g.71351504C>G	GRCh37
NC_000002.10:g.71205012C>G	NCBI36
NG_008977.1:g.10891G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244217.6:c.210G>C MANE Select	ENSP00000244217.5:p.Gly70=
ENST00000244217.5:c.210G>C	ENSP00000244217.5:p.Gly70=
ENST00000413592.5:c.78G>C	ENSP00000391140.1:p.Gly26=
ENST00000486135.1:c.-76G>C	ENSP00000441569.1:n.-76G>C
ENST00000494660.6:c.-76G>C	ENSP00000437361.1:n.-76G>C
NM_032601.3:c.210G>C	NP_115990.3:p.Gly70=
XM_005264613.2:c.210G>C	XP_005264670.1:p.Gly70=
XR_939729.1:n.279G>C
XR_939729.2:n.279G>C
NM_032601.4:c.210G>C MANE Select	NP_115990.3:p.Gly70=