Canonical Allele Identifier: CA91734638
Gene: EVC HGNC NCBI

Linked Data

dbSNP Id: rs559331894
gnomAD v2: 4-5712922-C-T
gnomAD v3: 4-5711195-C-T
gnomAD v4: 4-5711195-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.5711195C>T , CM000666.2:g.5711195C>T GRCh38
NC_000004.11:g.5712922C>T , CM000666.1:g.5712922C>T GRCh37
NC_000004.10:g.5763823C>T NCBI36
NG_008843.1:g.4999C>T
NG_015821.1:g.3354G>A

Transcript Alleles

HGVS Amino-acid Change
XM_006713865.2:c.-186C>T XP_006713928.1:n.-186C>T
XM_006713866.2:c.-186C>T XP_006713929.1:n.-186C>T
XM_011513419.1:c.-186C>T XP_011511721.1:n.-186C>T
XR_427473.2:n.5C>T
XR_427475.2:n.5C>T
XR_427476.2:n.5C>T
XR_924920.1:n.5C>T
XR_924921.1:n.5C>T
XR_924922.1:n.5C>T
XR_924923.1:n.5C>T
XR_924924.1:n.5C>T
XR_924925.1:n.5C>T
XR_924926.1:n.5C>T
XR_924927.1:n.5C>T
XR_924928.1:n.7C>T