Canonical Allele Identifier: CA2669805788
Gene: EVC HGNC NCBI

Linked Data

gnomAD v4: 4-5711196-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.5711196T>A , CM000666.2:g.5711196T>A GRCh38
NC_000004.11:g.5712923T>A , CM000666.1:g.5712923T>A GRCh37
NC_000004.10:g.5763824T>A NCBI36
NG_008843.1:g.5000T>A
NG_015821.1:g.3353A>T

Transcript Alleles

HGVS Amino-acid Change
XM_006713865.2:c.-185T>A XP_006713928.1:n.-185T>A
XM_006713866.2:c.-185T>A XP_006713929.1:n.-185T>A
XM_011513419.1:c.-185T>A XP_011511721.1:n.-185T>A
XR_427473.2:n.6T>A
XR_427475.2:n.6T>A
XR_427476.2:n.6T>A
XR_924920.1:n.6T>A
XR_924921.1:n.6T>A
XR_924922.1:n.6T>A
XR_924923.1:n.6T>A
XR_924924.1:n.6T>A
XR_924925.1:n.6T>A
XR_924926.1:n.6T>A
XR_924927.1:n.6T>A
XR_924928.1:n.8T>A