Canonical Allele Identifier: CA426691520
Gene: MCEE HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.71351576A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124446A>C , CM000664.2:g.71124446A>C GRCh38
NC_000002.11:g.71351576A>C , CM000664.1:g.71351576A>C GRCh37
NC_000002.10:g.71205084A>C NCBI36
NG_008977.1:g.10819T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000244217.6:c.138T>G MANE Select ENSP00000244217.5:p.Gly46=
ENST00000244217.5:c.138T>G ENSP00000244217.5:p.Gly46=
ENST00000413592.5:c.6T>G ENSP00000391140.1:p.Gly2=
ENST00000486135.1:c.-148T>G ENSP00000441569.1:n.-148T>G
ENST00000494660.6:c.-148T>G ENSP00000437361.1:n.-148T>G
NM_032601.3:c.138T>G NP_115990.3:p.Gly46=
XM_005264613.2:c.138T>G XP_005264670.1:p.Gly46=
XR_939729.1:n.207T>G
XR_939729.2:n.207T>G
NM_032601.4:c.138T>G MANE Select NP_115990.3:p.Gly46=
Search 100 bp 5'
Search 100 bp 3'