Canonical Allele Identifier: CA2576998213
Gene: MCEE HGNC NCBI

Linked Data

gnomAD v4: 2-71124596-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71124596T>A , CM000664.2:g.71124596T>A GRCh38
NC_000002.11:g.71351726T>A , CM000664.1:g.71351726T>A GRCh37
NC_000002.10:g.71205234T>A NCBI36
NG_008977.1:g.10669A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000244217.6:c.41-53A>T MANE Select ENSP00000244217.5:n.41-53A>T
ENST00000244217.5:c.41-53A>T ENSP00000244217.5:n.41-53A>T
ENST00000486135.1:c.-245-53A>T ENSP00000441569.1:n.-245-53A>T
ENST00000494660.6:c.-245-53A>T ENSP00000437361.1:n.-245-53A>T
NM_032601.3:c.41-53A>T NP_115990.3:n.41-53A>T
XM_005264613.2:c.41-53A>T XP_005264670.1:n.41-53A>T
XR_939729.1:n.110-53A>T
XR_939729.2:n.110-53A>T
NM_032601.4:c.41-53A>T MANE Select NP_115990.3:n.41-53A>T
Search 100 bp 5'
Search 100 bp 3'