Canonical Allele Identifier: CA2834926

Gene: EVC2

Linked Data

• ClinVar Variation Id: 1117883
• ClinVar RCV Id: RCV001446796
• dbSNP Id: rs758243772
• ExAC: 4:5630345 C / T
• gnomAD v2: 4-5630345-C-T
• gnomAD v3: 4-5628618-C-T
• gnomAD v4: 4-5628618-C-T
• COSMIC: COSM4125211 ; COSM4125212
• MyVariant Identifiers: chr4:g.5630345C>T (hg19) ; chr4:g.5628618C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5628618C>T , CM000666.2:g.5628618C>T	GRCh38
NC_000004.11:g.5630345C>T , CM000666.1:g.5630345C>T	GRCh37
NC_000004.10:g.5681246C>T	NCBI36
NG_015821.1:g.85931G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.1827G>A MANE Select	ENSP00000342144.5:p.Val609=
ENST00000310917.6:c.1587G>A	ENSP00000311683.2:p.Val529=
ENST00000344408.9:c.1827G>A	ENSP00000342144.5:p.Val609=
ENST00000475313.5:c.1587G>A	ENSP00000431981.1:p.Val529=
ENST00000509670.1:c.*220G>A	ENSP00000423876.1:n.*220G>A
NM_001166136.1:c.1587G>A	NP_001159608.1:p.Val529=
NM_147127.4:c.1827G>A	NP_667338.3:p.Val609=
XM_011513392.1:c.1836G>A	XP_011511694.1:p.Val612=
XM_011513393.1:c.1836G>A	XP_011511695.1:p.Val612=
XM_011513394.1:c.1596G>A	XP_011511696.1:p.Val532=
XM_017007736.1:c.1587G>A	XP_016863225.1:p.Val529=
XM_017007737.1:c.1587G>A	XP_016863226.1:p.Val529=
XM_017007738.1:c.1827G>A	XP_016863227.1:p.Val609=
XM_017007739.1:c.147G>A	XP_016863228.1:p.Val49=
XM_024453893.1:c.147G>A	XP_024309661.1:p.Val49=
XR_001741141.1:n.1892G>A
NM_147127.5:c.1827G>A MANE Select	NP_667338.3:p.Val609=
NM_001166136.2:c.1587G>A	NP_001159608.1:p.Val529=