Canonical Allele Identifier: CA1435469321
Gene: EVC HGNC NCBI

Linked Data

dbSNP Id: rs1433404009

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.5711192C>G , CM000666.2:g.5711192C>G GRCh38
NC_000004.11:g.5712919C>G , CM000666.1:g.5712919C>G GRCh37
NC_000004.10:g.5763820C>G NCBI36
NG_008843.1:g.4996C>G
NG_015821.1:g.3357G>C

Transcript Alleles

HGVS Amino-acid Change
XM_006713865.2:c.-189C>G XP_006713928.1:n.-189C>G
XM_006713866.2:c.-189C>G XP_006713929.1:n.-189C>G
XM_011513419.1:c.-189C>G XP_011511721.1:n.-189C>G
XR_427473.2:n.2C>G
XR_427475.2:n.2C>G
XR_427476.2:n.2C>G
XR_924920.1:n.2C>G
XR_924921.1:n.2C>G
XR_924922.1:n.2C>G
XR_924923.1:n.2C>G
XR_924924.1:n.2C>G
XR_924925.1:n.2C>G
XR_924926.1:n.2C>G
XR_924927.1:n.2C>G
XR_924928.1:n.4C>G