Canonical Allele Identifier: CA2669805782

Gene: EVC

Linked Data

• gnomAD v4: 4-5711193-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5711193T>C , CM000666.2:g.5711193T>C	GRCh38
NC_000004.11:g.5712920T>C , CM000666.1:g.5712920T>C	GRCh37
NC_000004.10:g.5763821T>C	NCBI36
NG_008843.1:g.4997T>C
NG_015821.1:g.3356A>G

Transcript Alleles

HGVS	Amino-acid Change
XM_006713865.2:c.-188T>C	XP_006713928.1:n.-188T>C
XM_006713866.2:c.-188T>C	XP_006713929.1:n.-188T>C
XM_011513419.1:c.-188T>C	XP_011511721.1:n.-188T>C
XR_427473.2:n.3T>C
XR_427475.2:n.3T>C
XR_427476.2:n.3T>C
XR_924920.1:n.3T>C
XR_924921.1:n.3T>C
XR_924922.1:n.3T>C
XR_924923.1:n.3T>C
XR_924924.1:n.3T>C
XR_924925.1:n.3T>C
XR_924926.1:n.3T>C
XR_924927.1:n.3T>C
XR_924928.1:n.5T>C