Canonical Allele Identifier: CA2834633

Gene: EVC2

Linked Data

• dbSNP Id: rs371698182
• ExAC: 4:5620243 C / A
• gnomAD v2: 4-5620243-C-A
• gnomAD v3: 4-5618516-C-A
• gnomAD v4: 4-5618516-C-A
• MyVariant Identifiers: chr4:g.5620243C>A (hg19) ; chr4:g.5618516C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5618516C>A , CM000666.2:g.5618516C>A	GRCh38
NC_000004.11:g.5620243C>A , CM000666.1:g.5620243C>A	GRCh37
NC_000004.10:g.5671144C>A	NCBI36
NG_015821.1:g.96033G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.2668G>T MANE Select	ENSP00000342144.5:p.Val890Leu
ENST00000310917.6:c.2428G>T	ENSP00000311683.2:p.Val810Leu
ENST00000344408.9:c.2668G>T	ENSP00000342144.5:p.Val890Leu
ENST00000475313.5:c.2428G>T	ENSP00000431981.1:p.Val810Leu
ENST00000509670.1:c.*1061G>T	ENSP00000423876.1:n.*1061G>T
NM_001166136.1:c.2428G>T	NP_001159608.1:p.Val810Leu
NM_147127.4:c.2668G>T	NP_667338.3:p.Val890Leu
XM_011513392.1:c.2677G>T	XP_011511694.1:p.Val893Leu
XM_011513393.1:c.2677G>T	XP_011511695.1:p.Val893Leu
XM_011513394.1:c.2437G>T	XP_011511696.1:p.Val813Leu
XM_017007736.1:c.2428G>T	XP_016863225.1:p.Val810Leu
XM_017007737.1:c.2428G>T	XP_016863226.1:p.Val810Leu
XM_017007738.1:c.2668G>T	XP_016863227.1:p.Val890Leu
XM_017007739.1:c.988G>T	XP_016863228.1:p.Val330Leu
XM_024453893.1:c.988G>T	XP_024309661.1:p.Val330Leu
XR_001741141.1:n.2733G>T
NM_147127.5:c.2668G>T MANE Select	NP_667338.3:p.Val890Leu
NM_001166136.2:c.2428G>T	NP_001159608.1:p.Val810Leu