Canonical Allele Identifier: CA2834920

Gene: EVC2

Linked Data

• ClinVar Variation Id: 1097412
• ClinVar RCV Id: RCV001419013
• dbSNP Id: rs139729159
• ExAC: 4:5630318 G / A
• gnomAD v2: 4-5630318-G-A
• gnomAD v3: 4-5628591-G-A
• gnomAD v4: 4-5628591-G-A
• MyVariant Identifiers: chr4:g.5630318G>A (hg19) ; chr4:g.5628591G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5628591G>A , CM000666.2:g.5628591G>A	GRCh38
NC_000004.11:g.5630318G>A , CM000666.1:g.5630318G>A	GRCh37
NC_000004.10:g.5681219G>A	NCBI36
NG_015821.1:g.85958C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.1854C>T MANE Select	ENSP00000342144.5:p.Ala618=
ENST00000310917.6:c.1614C>T	ENSP00000311683.2:p.Ala538=
ENST00000344408.9:c.1854C>T	ENSP00000342144.5:p.Ala618=
ENST00000475313.5:c.1614C>T	ENSP00000431981.1:p.Ala538=
ENST00000509670.1:c.*247C>T	ENSP00000423876.1:n.*247C>T
NM_001166136.1:c.1614C>T	NP_001159608.1:p.Ala538=
NM_147127.4:c.1854C>T	NP_667338.3:p.Ala618=
XM_011513392.1:c.1863C>T	XP_011511694.1:p.Ala621=
XM_011513393.1:c.1863C>T	XP_011511695.1:p.Ala621=
XM_011513394.1:c.1623C>T	XP_011511696.1:p.Ala541=
XM_017007736.1:c.1614C>T	XP_016863225.1:p.Ala538=
XM_017007737.1:c.1614C>T	XP_016863226.1:p.Ala538=
XM_017007738.1:c.1854C>T	XP_016863227.1:p.Ala618=
XM_017007739.1:c.174C>T	XP_016863228.1:p.Ala58=
XM_024453893.1:c.174C>T	XP_024309661.1:p.Ala58=
XR_001741141.1:n.1919C>T
NM_147127.5:c.1854C>T MANE Select	NP_667338.3:p.Ala618=
NM_001166136.2:c.1614C>T	NP_001159608.1:p.Ala538=