Canonical Allele Identifier: CA347188899
Gene: MCEE HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.71351523A>C (hg19) chr2:g.71124393A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124393A>C , CM000664.2:g.71124393A>C GRCh38
NC_000002.11:g.71351523A>C , CM000664.1:g.71351523A>C GRCh37
NC_000002.10:g.71205031A>C NCBI36
NG_008977.1:g.10872T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.191T>G MANE Select ENSP00000244217.5:p.Phe64Cys
ENST00000244217.5:c.191T>G ENSP00000244217.5:p.Phe64Cys
ENST00000413592.5:c.59T>G ENSP00000391140.1:p.Phe20Cys
ENST00000486135.1:c.-95T>G ENSP00000441569.1:n.-95T>G
ENST00000494660.6:c.-95T>G ENSP00000437361.1:n.-95T>G
NM_032601.3:c.191T>G NP_115990.3:p.Phe64Cys
XM_005264613.2:c.191T>G XP_005264670.1:p.Phe64Cys
XR_939729.1:n.260T>G
XR_939729.2:n.260T>G
NM_032601.4:c.191T>G MANE Select NP_115990.3:p.Phe64Cys
Search 100 bp 5'
Search 100 bp 3'