Canonical Allele Identifier: CA2669805785

Gene: EVC

Linked Data

• gnomAD v4: 4-5711194-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5711194C>A , CM000666.2:g.5711194C>A	GRCh38
NC_000004.11:g.5712921C>A , CM000666.1:g.5712921C>A	GRCh37
NC_000004.10:g.5763822C>A	NCBI36
NG_008843.1:g.4998C>A
NG_015821.1:g.3355G>T

Transcript Alleles

HGVS	Amino-acid Change
XM_006713865.2:c.-187C>A	XP_006713928.1:n.-187C>A
XM_006713866.2:c.-187C>A	XP_006713929.1:n.-187C>A
XM_011513419.1:c.-187C>A	XP_011511721.1:n.-187C>A
XR_427473.2:n.4C>A
XR_427475.2:n.4C>A
XR_427476.2:n.4C>A
XR_924920.1:n.4C>A
XR_924921.1:n.4C>A
XR_924922.1:n.4C>A
XR_924923.1:n.4C>A
XR_924924.1:n.4C>A
XR_924925.1:n.4C>A
XR_924926.1:n.4C>A
XR_924927.1:n.4C>A
XR_924928.1:n.6C>A