Canonical Allele Identifier: CA356147808

Gene: EVC2

Linked Data

• dbSNP Id: rs1297456994
• gnomAD v2: 4-5630410-G-C
• gnomAD v3: 4-5628683-G-C
• gnomAD v4: 4-5628683-G-C
• MyVariant Identifiers: chr4:g.5630410G>C (hg19) ; chr4:g.5628683G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5628683G>C , CM000666.2:g.5628683G>C	GRCh38
NC_000004.11:g.5630410G>C , CM000666.1:g.5630410G>C	GRCh37
NC_000004.10:g.5681311G>C	NCBI36
NG_015821.1:g.85866C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.1762C>G MANE Select	ENSP00000342144.5:p.Leu588Val
ENST00000310917.6:c.1522C>G	ENSP00000311683.2:p.Leu508Val
ENST00000344408.9:c.1762C>G	ENSP00000342144.5:p.Leu588Val
ENST00000475313.5:c.1522C>G	ENSP00000431981.1:p.Leu508Val
ENST00000509670.1:c.*155C>G	ENSP00000423876.1:n.*155C>G
NM_001166136.1:c.1522C>G	NP_001159608.1:p.Leu508Val
NM_147127.4:c.1762C>G	NP_667338.3:p.Leu588Val
XM_011513392.1:c.1771C>G	XP_011511694.1:p.Leu591Val
XM_011513393.1:c.1771C>G	XP_011511695.1:p.Leu591Val
XM_011513394.1:c.1531C>G	XP_011511696.1:p.Leu511Val
XM_017007736.1:c.1522C>G	XP_016863225.1:p.Leu508Val
XM_017007737.1:c.1522C>G	XP_016863226.1:p.Leu508Val
XM_017007738.1:c.1762C>G	XP_016863227.1:p.Leu588Val
XM_017007739.1:c.82C>G	XP_016863228.1:p.Leu28Val
XM_024453893.1:c.82C>G	XP_024309661.1:p.Leu28Val
XR_001741141.1:n.1827C>G
NM_147127.5:c.1762C>G MANE Select	NP_667338.3:p.Leu588Val
NM_001166136.2:c.1522C>G	NP_001159608.1:p.Leu508Val